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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:PTPRZ1-CPED1 (FusionGDB2 ID:70140)

Fusion Gene Summary for PTPRZ1-CPED1

check button Fusion gene summary
Fusion gene informationFusion gene name: PTPRZ1-CPED1
Fusion gene ID: 70140
HgeneTgene
Gene symbol

PTPRZ1

CPED1

Gene ID

5803

79974

Gene nameprotein tyrosine phosphatase receptor type Z1cadherin like and PC-esterase domain containing 1
SynonymsHPTPZ|HPTPzeta|PTP-ZETA|PTP18|PTPRZ|PTPZ|R-PTP-zeta-2|RPTPB|RPTPbeta|phosphacanC7orf58
Cytomap

7q31.32

7q31.31

Type of geneprotein-codingprotein-coding
Descriptionreceptor-type tyrosine-protein phosphatase zetaprotein tyrosine phosphatase, receptor-type, Z polypeptide 1protein tyrosine phosphatase, receptor-type, zeta polypeptide 1protein-tyrosine phosphatase receptor type Z polypeptide 2receptor-type tyrosine cadherin-like and PC-esterase domain-containing protein 1
Modification date2020031320200313
UniProtAcc.

A4D0V7

Ensembl transtripts involved in fusion geneENST00000393386, ENST00000449182, 
ENST00000483028, 
ENST00000310396, 
ENST00000450913, ENST00000423795, 
ENST00000495036, ENST00000340646, 
Fusion gene scores* DoF score15 X 14 X 7=14709 X 8 X 5=360
# samples 199
** MAII scorelog2(19/1470*10)=-2.95174483139278
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/360*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PTPRZ1 [Title/Abstract] AND CPED1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPTPRZ1(121513611)-CPED1(120935494), # samples:1
Anticipated loss of major functional domain due to fusion event.PTPRZ1-CPED1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PTPRZ1-CPED1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PTPRZ1-CPED1 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 buttonFusion gene breakpoints across PTPRZ1 (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 CPED1 (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
ChimerDB4LGGTCGA-TM-A84J-01APTPRZ1chr7

121513611

+CPED1chr7

120935494

+


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Fusion Gene ORF analysis for PTPRZ1-CPED1

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-shiftENST00000393386ENST00000310396PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
5CDS-intronENST00000393386ENST00000450913PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
5CDS-intronENST00000393386ENST00000423795PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
5CDS-intronENST00000393386ENST00000495036PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
5CDS-intronENST00000393386ENST00000340646PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
Frame-shiftENST00000449182ENST00000310396PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
5CDS-intronENST00000449182ENST00000450913PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
5CDS-intronENST00000449182ENST00000423795PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
5CDS-intronENST00000449182ENST00000495036PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
5CDS-intronENST00000449182ENST00000340646PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
intron-3CDSENST00000483028ENST00000310396PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
intron-intronENST00000483028ENST00000450913PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
intron-intronENST00000483028ENST00000423795PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
intron-intronENST00000483028ENST00000495036PTPRZ1chr7

121513611

+CPED1chr7

120935494

+
intron-intronENST00000483028ENST00000340646PTPRZ1chr7

121513611

+CPED1chr7

120935494

+

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 PTPRZ1-CPED1


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)
PTPRZ1chr7121513611+CPED1chr7120935493+0.959561350.040438615
PTPRZ1chr7121513611+CPED1chr7120935493+0.959561350.040438615

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 PTPRZ1-CPED1


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
.CPED1

A4D0V7

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.

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 PTPRZ1-CPED1


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 PTPRZ1-CPED1


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 PTPRZ1-CPED1


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 PTPRZ1-CPED1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePTPRZ1C0036341Schizophrenia3PSYGENET
HgenePTPRZ1C0004681Bagassosis1CTD_human
HgenePTPRZ1C0032273Pneumoconiosis1CTD_human
HgenePTPRZ1C0079487Helicobacter Infections1CTD_human
HgenePTPRZ1C1838332HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO1GENOMICS_ENGLAND
TgeneCPED1C0022336Creutzfeldt-Jakob disease1CTD_human
TgeneCPED1C0376329New Variant Creutzfeldt-Jakob Disease1CTD_human
TgeneCPED1C0751254Creutzfeldt-Jakob Disease, Familial1CTD_human