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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:AASDHPPT-CASP1 (FusionGDB2 ID:HG60496TG834)

Fusion Gene Summary for AASDHPPT-CASP1

check button Fusion gene summary
Fusion gene informationFusion gene name: AASDHPPT-CASP1
Fusion gene ID: hg60496tg834
HgeneTgene
Gene symbol

AASDHPPT

CASP1

Gene ID

60496

834

Gene nameaminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferasecaspase 1
SynonymsAASD-PPT|ACPS|CGI-80|LYS2|LYS5ICE|IL1BC|P45
Cytomap('AASDHPPT')('CASP1')

11q22.3

11q22.3

Type of geneprotein-codingprotein-coding
DescriptionL-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase4'-phosphopantetheinyl transferaseLYS5 orthologalpha-aminoadipic semialdehyde dehydrogenase-phosphopantetheinyl transferaseholo ACP synthaseholo-[acyl-carrier-protein] synthasecaspase-1CASP1 nirs variant 1IL-1 beta-converting enzymeIL1B-convertasecaspase 1, apoptosis-related cysteine peptidaseinterleukin 1, beta, convertaseinterleukin 1-B converting enzyme
Modification date2020031320200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000278618, 
Fusion gene scores* DoF score3 X 1 X 2=65 X 4 X 4=80
# samples 25
** MAII scorelog2(2/6*10)=1.73696559416621log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: AASDHPPT [Title/Abstract] AND CASP1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointAASDHPPT(105950419)-CASP1(104905201), # samples:1
Anticipated loss of major functional domain due to fusion event.AASDHPPT-CASP1 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
AASDHPPT-CASP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
AASDHPPT-CASP1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
TgeneCASP1

GO:0006508

proteolysis

12888622|24548080

TgeneCASP1

GO:0016540

protein autoprocessing

11821383

TgeneCASP1

GO:0050718

positive regulation of interleukin-1 beta secretion

11432859|11821383

TgeneCASP1

GO:0071310

cellular response to organic substance

19158679



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
ChimerDB4BLCATCGA-CF-A1HS-01AAASDHPPTchr11

105950419

+CASP1chr11

104905201

-


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Fusion Gene ORF analysis for AASDHPPT-CASP1

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-5UTRENST00000278618ENST00000353247AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000393136AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000415981AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000436863AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000446369AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000525825AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000527979AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000531166AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000533400AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000534497AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000593315AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000594519AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-5UTRENST00000278618ENST00000598974AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
5CDS-intronENST00000278618ENST00000528974AASDHPPTchr11

105950419

+CASP1chr11

104905201

-
Frame-shiftENST00000278618ENST00000526568AASDHPPTchr11

105950419

+CASP1chr11

104905201

-

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 AASDHPPT-CASP1


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 AASDHPPT-CASP1


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/:105950419/:104905201)
- 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 AASDHPPT-CASP1


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 AASDHPPT-CASP1


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 AASDHPPT-CASP1


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 AASDHPPT-CASP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC0001925Albuminuria1CTD_human
TgeneC0020517Hypersensitivity1CTD_human
TgeneC0021368Inflammation1CTD_human
TgeneC0021655Insulin Resistance1CTD_human
TgeneC0022658Kidney Diseases1CTD_human
TgeneC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneC0026769Multiple Sclerosis1CTD_human
TgeneC0027055Myocardial Reperfusion Injury1CTD_human
TgeneC0028754Obesity1CTD_human
TgeneC0032285Pneumonia1CTD_human
TgeneC0032300Lobar Pneumonia1CTD_human
TgeneC0038220Status Epilepticus1CTD_human
TgeneC0270823Petit mal status1CTD_human
TgeneC0311335Grand Mal Status Epilepticus1CTD_human
TgeneC0393734Complex Partial Status Epilepticus1CTD_human
TgeneC0598608Hyperhomocysteinemia1CTD_human
TgeneC0751324Multiple Sclerosis, Acute Fulminating1CTD_human
TgeneC0751522Status Epilepticus, Subclinical1CTD_human
TgeneC0751523Non-Convulsive Status Epilepticus1CTD_human
TgeneC0751524Simple Partial Status Epilepticus1CTD_human
TgeneC0887898Experimental Lung Inflammation1CTD_human
TgeneC0920563Insulin Sensitivity1CTD_human
TgeneC1527304Allergic Reaction1CTD_human
TgeneC1862939AMYOTROPHIC LATERAL SCLEROSIS 11CTD_human
TgeneC1862941Amyotrophic Lateral Sclerosis, Sporadic1CTD_human
TgeneC3714636Pneumonitis1CTD_human
TgeneC4551993Amyotrophic Lateral Sclerosis, Familial1CTD_human