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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:PNRC1-EZR (FusionGDB2 ID:66384)

Fusion Gene Summary for PNRC1-EZR

check button Fusion gene summary
Fusion gene informationFusion gene name: PNRC1-EZR
Fusion gene ID: 66384
HgeneTgene
Gene symbol

PNRC1

EZR

Gene ID

10957

7430

Gene nameproline rich nuclear receptor coactivator 1ezrin
SynonymsB4-2|PNAS-145|PROL2|PRR2CVIL|CVL|HEL-S-105|VIL2
Cytomap

6q15

6q25.3

Type of geneprotein-codingprotein-coding
Descriptionproline-rich nuclear receptor coactivator 1proline rich 2 proteinproline-rich polypeptide 2proline-rich protein 2proline-rich protein with nuclear targeting signalprotein B4-2ezrincytovillin 2epididymis secretory protein Li 105p81villin 2 (ezrin)
Modification date2020031320200322
UniProtAcc.

P15311

Ensembl transtripts involved in fusion geneENST00000369472, ENST00000336032, 
ENST00000354922, 
ENST00000337147, 
ENST00000367075, ENST00000392177, 
ENST00000476189, 
Fusion gene scores* DoF score5 X 3 X 2=3025 X 24 X 6=3600
# samples 527
** MAII scorelog2(5/30*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(27/3600*10)=-3.73696559416621
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PNRC1 [Title/Abstract] AND EZR [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPNRC1(89790532)-EZR(159192300), # 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
TgeneEZR

GO:0048015

phosphatidylinositol-mediated signaling

25591774

TgeneEZR

GO:0051017

actin filament bundle assembly

10793131


check buttonFusion gene breakpoints across PNRC1 (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 EZR (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
ChiTaRS5.0N/ABM761260PNRC1chr6

89790532

+EZRchr6

159192300

-
ChiTaRS5.0N/ABM762912PNRC1chr6

89790532

+EZRchr6

159192300

-
ChiTaRS5.0N/ABM846053PNRC1chr6

89790532

+EZRchr6

159192300

-


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Fusion Gene ORF analysis for PNRC1-EZR

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
5UTR-3CDSENST00000369472ENST00000337147PNRC1chr6

89790532

+EZRchr6

159192300

-
5UTR-3CDSENST00000369472ENST00000367075PNRC1chr6

89790532

+EZRchr6

159192300

-
5UTR-3CDSENST00000369472ENST00000392177PNRC1chr6

89790532

+EZRchr6

159192300

-
5UTR-intronENST00000369472ENST00000476189PNRC1chr6

89790532

+EZRchr6

159192300

-
5UTR-3CDSENST00000336032ENST00000337147PNRC1chr6

89790532

+EZRchr6

159192300

-
5UTR-3CDSENST00000336032ENST00000367075PNRC1chr6

89790532

+EZRchr6

159192300

-
5UTR-3CDSENST00000336032ENST00000392177PNRC1chr6

89790532

+EZRchr6

159192300

-
5UTR-intronENST00000336032ENST00000476189PNRC1chr6

89790532

+EZRchr6

159192300

-
intron-3CDSENST00000354922ENST00000337147PNRC1chr6

89790532

+EZRchr6

159192300

-
intron-3CDSENST00000354922ENST00000367075PNRC1chr6

89790532

+EZRchr6

159192300

-
intron-3CDSENST00000354922ENST00000392177PNRC1chr6

89790532

+EZRchr6

159192300

-
intron-intronENST00000354922ENST00000476189PNRC1chr6

89790532

+EZRchr6

159192300

-

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 PNRC1-EZR


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)

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 PNRC1-EZR


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
.EZR

P15311

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: Probably involved in connections of major cytoskeletal structures to the plasma membrane. In epithelial cells, required for the formation of microvilli and membrane ruffles on the apical pole. Along with PLEKHG6, required for normal macropinocytosis. {ECO:0000269|PubMed:17881735, ECO:0000269|PubMed:18270268, ECO:0000269|PubMed:19111582}.

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 PNRC1-EZR


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 PNRC1-EZR


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 PNRC1-EZR


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 PNRC1-EZR


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePNRC1C0019193Hepatitis, Toxic1CTD_human
HgenePNRC1C0860207Drug-Induced Liver Disease1CTD_human
HgenePNRC1C1262760Hepatitis, Drug-Induced1CTD_human
HgenePNRC1C3658290Drug-Induced Acute Liver Injury1CTD_human
HgenePNRC1C4277682Chemical and Drug Induced Liver Injury1CTD_human
HgenePNRC1C4279912Chemically-Induced Liver Toxicity1CTD_human
TgeneEZRC0033578Prostatic Neoplasms3CTD_human
TgeneEZRC0376358Malignant neoplasm of prostate3CTD_human
TgeneEZRC0007097Carcinoma1CTD_human
TgeneEZRC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneEZRC0024667Animal Mammary Neoplasms1CTD_human
TgeneEZRC0024668Mammary Neoplasms, Experimental1CTD_human
TgeneEZRC0027627Neoplasm Metastasis1CTD_human
TgeneEZRC0029408Degenerative polyarthritis1CTD_human
TgeneEZRC0086743Osteoarthrosis Deformans1CTD_human
TgeneEZRC0205696Anaplastic carcinoma1CTD_human
TgeneEZRC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneEZRC0205698Undifferentiated carcinoma1CTD_human
TgeneEZRC0205699Carcinomatosis1CTD_human
TgeneEZRC1257925Mammary Carcinoma, Animal1CTD_human