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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:PLEKHA5-SLCO1B1 (FusionGDB2 ID:65781)

Fusion Gene Summary for PLEKHA5-SLCO1B1

check button Fusion gene summary
Fusion gene informationFusion gene name: PLEKHA5-SLCO1B1
Fusion gene ID: 65781
HgeneTgene
Gene symbol

PLEKHA5

SLCO1B1

Gene ID

54477

10599

Gene namepleckstrin homology domain containing A5solute carrier organic anion transporter family member 1B1
SynonymsPEPP-2|PEPP2HBLRR|LST-1|LST1|OATP-C|OATP1B1|OATP2|OATPC|SLC21A6
Cytomap

12p12.3

12p12.1

Type of geneprotein-codingprotein-coding
Descriptionpleckstrin homology domain-containing family A member 5PH domain-containing family A member 5phosphoinositol 3-phosphate-binding protein-2pleckstrin homology domain containing, family A member 5solute carrier organic anion transporter family member 1B1OATP-2liver-specific organic anion transporter 1sodium-independent organic anion-transporting polypeptide 2solute carrier family 21 (organic anion transporter), member 6
Modification date2020032020200313
UniProtAcc.

Q9Y6L6

Ensembl transtripts involved in fusion geneENST00000309364, ENST00000359180, 
ENST00000317589, ENST00000355397, 
ENST00000429027, ENST00000539256, 
ENST00000299275, ENST00000538714, 
ENST00000543806, ENST00000424268, 
ENST00000540972, ENST00000510738, 
ENST00000256958, 
Fusion gene scores* DoF score19 X 17 X 12=38767 X 7 X 5=245
# samples 239
** MAII scorelog2(23/3876*10)=-4.07486280447071
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/245*10)=-1.4447848426729
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PLEKHA5 [Title/Abstract] AND SLCO1B1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPLEKHA5(19285384)-SLCO1B1(21325584), # samples:2
Anticipated loss of major functional domain due to fusion event.PLEKHA5-SLCO1B1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PLEKHA5-SLCO1B1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PLEKHA5-SLCO1B1 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

check buttonFusion gene breakpoints across PLEKHA5 (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 SLCO1B1 (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
ChimerDB4OVTCGA-61-2102-01APLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
ChimerDB4OVTCGA-61-2102-01APLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+


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Fusion Gene ORF analysis for PLEKHA5-SLCO1B1

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
Frame-shiftENST00000309364ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
Frame-shiftENST00000359180ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
Frame-shiftENST00000317589ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
Frame-shiftENST00000355397ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
Frame-shiftENST00000429027ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
5UTR-3CDSENST00000539256ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
Frame-shiftENST00000299275ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
Frame-shiftENST00000538714ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
intron-3CDSENST00000543806ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
intron-3CDSENST00000424268ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
Frame-shiftENST00000540972ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+
intron-3CDSENST00000510738ENST00000256958PLEKHA5chr12

19285384

+SLCO1B1chr12

21325584

+

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 PLEKHA5-SLCO1B1


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)
PLEKHA5chr1219285384+SLCO1B1chr1221325583+0.0003196210.9996804
PLEKHA5chr1219285384+SLCO1B1chr1221325583+0.0003196210.9996804

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.

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Fusion Protein Features for PLEKHA5-SLCO1B1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.SLCO1B1

Q9Y6L6

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Mediates the Na(+)-independent uptake of organic anions such as pravastatin, taurocholate, methotrexate, dehydroepiandrosterone sulfate, 17-beta-glucuronosyl estradiol, estrone sulfate, prostaglandin E2, thromboxane B2, leukotriene C3, leukotriene E4, thyroxine and triiodothyronine. Involved in the clearance of bile acids and organic anions from the liver. {ECO:0000269|PubMed:10358072, ECO:0000269|PubMed:10601278, ECO:0000269|PubMed:12196548, ECO:0000269|PubMed:22232210}.

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 PLEKHA5-SLCO1B1


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 PLEKHA5-SLCO1B1


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 PLEKHA5-SLCO1B1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneSLCO1B1Q9Y6L6DB01211ClarithromycinSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01211ClarithromycinSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01211ClarithromycinSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01211ClarithromycinSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01211ClarithromycinSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01211ClarithromycinSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01241GemfibrozilInhibitorSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01241GemfibrozilInhibitorSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01241GemfibrozilInhibitorSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01241GemfibrozilInhibitorSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01241GemfibrozilInhibitorSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB01241GemfibrozilInhibitorSmall moleculeApproved
TgeneSLCO1B1Q9Y6L6DB05521TelaprevirInhibitorSmall moleculeApproved|Withdrawn
TgeneSLCO1B1Q9Y6L6DB05521TelaprevirInhibitorSmall moleculeApproved|Withdrawn
TgeneSLCO1B1Q9Y6L6DB05521TelaprevirInhibitorSmall moleculeApproved|Withdrawn
TgeneSLCO1B1Q9Y6L6DB05521TelaprevirInhibitorSmall moleculeApproved|Withdrawn
TgeneSLCO1B1Q9Y6L6DB05521TelaprevirInhibitorSmall moleculeApproved|Withdrawn
TgeneSLCO1B1Q9Y6L6DB05521TelaprevirInhibitorSmall moleculeApproved|Withdrawn

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Related Diseases for PLEKHA5-SLCO1B1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePLEKHA5C0008924Cleft upper lip1GENOMICS_ENGLAND
TgeneSLCO1B1C0026848Myopathy5CTD_human
TgeneSLCO1B1C0006142Malignant neoplasm of breast1CTD_human
TgeneSLCO1B1C0013221Drug toxicity1CTD_human
TgeneSLCO1B1C0041755Adverse reaction to drug1CTD_human
TgeneSLCO1B1C0220991Rotor Syndrome1CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneSLCO1B1C0678222Breast Carcinoma1CTD_human
TgeneSLCO1B1C1257931Mammary Neoplasms, Human1CTD_human
TgeneSLCO1B1C1458155Mammary Neoplasms1CTD_human
TgeneSLCO1B1C4016905HYPERBILIRUBINEMIA, ROTOR TYPE, DIGENIC1GENOMICS_ENGLAND
TgeneSLCO1B1C4704874Mammary Carcinoma, Human1CTD_human