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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:ACYP1-LRRC59 (FusionGDB2 ID:HG97TG55379)

Fusion Gene Summary for ACYP1-LRRC59

check button Fusion gene summary
Fusion gene informationFusion gene name: ACYP1-LRRC59
Fusion gene ID: hg97tg55379
HgeneTgene
Gene symbol

ACYP1

LRRC59

Gene ID

97

55379

Gene nameacylphosphatase 1leucine rich repeat containing 59
SynonymsACYPEPRO1855|p34
Cytomap('ACYP1')('LRRC59')

14q24.3

17q21.33

Type of geneprotein-codingprotein-coding
Descriptionacylphosphatase-1acylphosphatase 1, erythrocyte (common) typeacylphosphatase, erythrocyte isozymeacylphosphatase, organ-common type isozymeacylphosphate phosphohydrolase 1leucine-rich repeat-containing protein 59ribosome-binding protein p34
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000238618, ENST00000357971, 
ENST00000555135, ENST00000555463, 
ENST00000555694, ENST00000553302, 
Fusion gene scores* DoF score1 X 1 X 1=17 X 4 X 6=168
# samples 17
** MAII scorelog2(1/1*10)=3.32192809488736log2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ACYP1 [Title/Abstract] AND LRRC59 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointACYP1(75530173)-LRRC59(48460596), # samples:1
Anticipated loss of major functional domain due to fusion event.ACYP1-LRRC59 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
ACYP1-LRRC59 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 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-BR-A4QI-01AACYP1chr14

75530173

-LRRC59chr17

48460596

-


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Fusion Gene ORF analysis for ACYP1-LRRC59

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-intronENST00000238618ENST00000576448ACYP1chr14

75530173

-LRRC59chr17

48460596

-
5CDS-intronENST00000357971ENST00000576448ACYP1chr14

75530173

-LRRC59chr17

48460596

-
5CDS-intronENST00000555135ENST00000576448ACYP1chr14

75530173

-LRRC59chr17

48460596

-
5CDS-intronENST00000555463ENST00000576448ACYP1chr14

75530173

-LRRC59chr17

48460596

-
5CDS-intronENST00000555694ENST00000576448ACYP1chr14

75530173

-LRRC59chr17

48460596

-
Frame-shiftENST00000238618ENST00000225972ACYP1chr14

75530173

-LRRC59chr17

48460596

-
Frame-shiftENST00000357971ENST00000225972ACYP1chr14

75530173

-LRRC59chr17

48460596

-
Frame-shiftENST00000555135ENST00000225972ACYP1chr14

75530173

-LRRC59chr17

48460596

-
Frame-shiftENST00000555463ENST00000225972ACYP1chr14

75530173

-LRRC59chr17

48460596

-
Frame-shiftENST00000555694ENST00000225972ACYP1chr14

75530173

-LRRC59chr17

48460596

-
intron-3CDSENST00000553302ENST00000225972ACYP1chr14

75530173

-LRRC59chr17

48460596

-
intron-intronENST00000553302ENST00000576448ACYP1chr14

75530173

-LRRC59chr17

48460596

-

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 ACYP1-LRRC59


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)


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Fusion Protein Features for ACYP1-LRRC59


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/:75530173/:48460596)
- 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 ACYP1-LRRC59


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 ACYP1-LRRC59


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 ACYP1-LRRC59


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 ACYP1-LRRC59


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneC0017636Glioblastoma1CTD_human
TgeneC0024232Lymphatic Metastasis1CTD_human
TgeneC0334588Giant Cell Glioblastoma1CTD_human
TgeneC0919267ovarian neoplasm1CTD_human
TgeneC1140680Malignant neoplasm of ovary1CTD_human
TgeneC1621958Glioblastoma Multiforme1CTD_human
TgeneC2239176Liver carcinoma1CTD_human