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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:PABPC1-RLIM (FusionGDB2 ID:HG26986TG51132)

Fusion Gene Summary for PABPC1-RLIM

check button Fusion gene summary
Fusion gene informationFusion gene name: PABPC1-RLIM
Fusion gene ID: hg26986tg51132
HgeneTgene
Gene symbol

PABPC1

RLIM

Gene ID

26986

51132

Gene namepoly(A) binding protein cytoplasmic 1ring finger protein, LIM domain interacting
SynonymsPAB1|PABP|PABP1|PABPC2|PABPL1MRX61|NY-REN-43|RNF12|TOKAS
Cytomap('PABPC1')('RLIM')

8q22.3

Xq13.2

Type of geneprotein-codingprotein-coding
Descriptionpolyadenylate-binding protein 1poly(A) binding protein, cytoplasmic 2E3 ubiquitin-protein ligase RLIME3 ubiquitin-protein ligase RNF12LIM domain-interacting RING finger proteinR-LIMRING finger LIM domain-binding proteinRING-type E3 ubiquitin transferase RLIMrenal carcinoma antigen NY-REN-43ring finger protein 12rin
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000318607, ENST00000519004, 
ENST00000522387, ENST00000519596, 
ENST00000318607, ENST00000519004, 
ENST00000522387, ENST00000519596, 
Fusion gene scores* DoF score31 X 28 X 11=95483 X 5 X 4=60
# samples 375
** MAII scorelog2(37/9548*10)=-4.68960139056546
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PABPC1 [Title/Abstract] AND RLIM [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPABPC1(101717154)-RLIM(73803072), # samples:3
PABPC1(101718879)-RLIM(73803377), # samples:3
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
HgenePABPC1

GO:2000623

negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay

18447585

TgeneRLIM

GO:0060816

random inactivation of X chromosome

19945382



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
ChimerDB4BRCATCGA-A8-A07O-01APABPC1chr8

101717154

-RLIMchrX

73803072

-
ChimerDB4BRCATCGA-A8-A092-01APABPC1chr8

101717154

-RLIMchrX

73803072

-
ChimerDB4BRCATCGA-B6-A0IE-01APABPC1chr8

101717154

-RLIMchrX

73803072

-
ChimerDB4GBMTCGA-06-5858-01APABPC1chr8

101718993

-RLIMchrX

73803327

-
ChiTaRS5.0N/AAX341383PABPC1chr8

101718879

-RLIMchrX

73803377

-
ChiTaRS5.0N/ACF139428PABPC1chr8

101718879

-RLIMchrX

73803377

-
ChiTaRS5.0N/ACF145721PABPC1chr8

101718879

-RLIMchrX

73803377

-


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Fusion Gene ORF analysis for PABPC1-RLIM

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-intronENST00000318607ENST00000332687PABPC1chr8

101717154

-RLIMchrX

73803072

-
5CDS-intronENST00000318607ENST00000332687PABPC1chr8

101718879

-RLIMchrX

73803377

-
5CDS-intronENST00000318607ENST00000349225PABPC1chr8

101717154

-RLIMchrX

73803072

-
5CDS-intronENST00000318607ENST00000349225PABPC1chr8

101718879

-RLIMchrX

73803377

-
5CDS-intronENST00000519004ENST00000332687PABPC1chr8

101717154

-RLIMchrX

73803072

-
5CDS-intronENST00000519004ENST00000332687PABPC1chr8

101718879

-RLIMchrX

73803377

-
5CDS-intronENST00000519004ENST00000349225PABPC1chr8

101717154

-RLIMchrX

73803072

-
5CDS-intronENST00000519004ENST00000349225PABPC1chr8

101718879

-RLIMchrX

73803377

-
5CDS-intronENST00000522387ENST00000332687PABPC1chr8

101717154

-RLIMchrX

73803072

-
5CDS-intronENST00000522387ENST00000332687PABPC1chr8

101718879

-RLIMchrX

73803377

-
5CDS-intronENST00000522387ENST00000349225PABPC1chr8

101717154

-RLIMchrX

73803072

-
5CDS-intronENST00000522387ENST00000349225PABPC1chr8

101718879

-RLIMchrX

73803377

-
intron-intronENST00000318607ENST00000332687PABPC1chr8

101718993

-RLIMchrX

73803327

-
intron-intronENST00000318607ENST00000349225PABPC1chr8

101718993

-RLIMchrX

73803327

-
intron-intronENST00000519004ENST00000332687PABPC1chr8

101718993

-RLIMchrX

73803327

-
intron-intronENST00000519004ENST00000349225PABPC1chr8

101718993

-RLIMchrX

73803327

-
intron-intronENST00000519596ENST00000332687PABPC1chr8

101717154

-RLIMchrX

73803072

-
intron-intronENST00000519596ENST00000332687PABPC1chr8

101718993

-RLIMchrX

73803327

-
intron-intronENST00000519596ENST00000332687PABPC1chr8

101718879

-RLIMchrX

73803377

-
intron-intronENST00000519596ENST00000349225PABPC1chr8

101717154

-RLIMchrX

73803072

-
intron-intronENST00000519596ENST00000349225PABPC1chr8

101718993

-RLIMchrX

73803327

-
intron-intronENST00000519596ENST00000349225PABPC1chr8

101718879

-RLIMchrX

73803377

-
intron-intronENST00000522387ENST00000332687PABPC1chr8

101718993

-RLIMchrX

73803327

-
intron-intronENST00000522387ENST00000349225PABPC1chr8

101718993

-RLIMchrX

73803327

-

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 PABPC1-RLIM


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 PABPC1-RLIM


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/:101717154/:73803072)
- 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 PABPC1-RLIM


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 PABPC1-RLIM


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 PABPC1-RLIM


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 PABPC1-RLIM


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePABPC1C0005684Malignant neoplasm of urinary bladder1CTD_human
HgenePABPC1C0005695Bladder Neoplasm1CTD_human
HgenePABPC1C0006142Malignant neoplasm of breast1CTD_human
HgenePABPC1C0007138Carcinoma, Transitional Cell1CTD_human
HgenePABPC1C0678222Breast Carcinoma1CTD_human
HgenePABPC1C1257931Mammary Neoplasms, Human1CTD_human
HgenePABPC1C1458155Mammary Neoplasms1CTD_human
HgenePABPC1C4704874Mammary Carcinoma, Human1CTD_human
TgeneC4283894MENTAL RETARDATION, X-LINKED 613CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneC3714756Intellectual Disability2GENOMICS_ENGLAND
TgeneC0033578Prostatic Neoplasms1CTD_human
TgeneC0376358Malignant neoplasm of prostate1CTD_human