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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:PFDN1-HBEGF (FusionGDB2 ID:63987)

Fusion Gene Summary for PFDN1-HBEGF

check button Fusion gene summary
Fusion gene informationFusion gene name: PFDN1-HBEGF
Fusion gene ID: 63987
HgeneTgene
Gene symbol

PFDN1

HBEGF

Gene ID

5201

1839

Gene nameprefoldin subunit 1heparin binding EGF like growth factor
SynonymsPDF|PFD1DTR|DTS|DTSF|HEGFL
Cytomap

5q31.3

5q31.3

Type of geneprotein-codingprotein-coding
Descriptionprefoldin subunit 1prefoldin 1proheparin-binding EGF-like growth factordiphtheria toxin receptor (heparin-binding EGF-like growth factor)diphtheria toxin receptor (heparin-binding epidermal growth factor-like growth factor)heparin-binding epidermal growth factor
Modification date2020031320200313
UniProtAcc.

Q99075

Ensembl transtripts involved in fusion geneENST00000261813, ENST00000514611, 
ENST00000510217, ENST00000524074, 
ENST00000230990, ENST00000507104, 
Fusion gene scores* DoF score3 X 3 X 3=271 X 1 X 1=1
# samples 31
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: PFDN1 [Title/Abstract] AND HBEGF [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPFDN1(139680001)-HBEGF(139715612), # samples:1
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

check buttonFusion gene breakpoints across PFDN1 (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 HBEGF (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
ChimerDB4ESCATCGA-L5-A8NEPFDN1chr5

139680001

-HBEGFchr5

139715612

-


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Fusion Gene ORF analysis for PFDN1-HBEGF

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
In-frameENST00000261813ENST00000230990PFDN1chr5

139680001

-HBEGFchr5

139715612

-
In-frameENST00000261813ENST00000507104PFDN1chr5

139680001

-HBEGFchr5

139715612

-
5UTR-3CDSENST00000514611ENST00000230990PFDN1chr5

139680001

-HBEGFchr5

139715612

-
5UTR-3CDSENST00000514611ENST00000507104PFDN1chr5

139680001

-HBEGFchr5

139715612

-
intron-3CDSENST00000510217ENST00000230990PFDN1chr5

139680001

-HBEGFchr5

139715612

-
intron-3CDSENST00000510217ENST00000507104PFDN1chr5

139680001

-HBEGFchr5

139715612

-
In-frameENST00000524074ENST00000230990PFDN1chr5

139680001

-HBEGFchr5

139715612

-
In-frameENST00000524074ENST00000507104PFDN1chr5

139680001

-HBEGFchr5

139715612

-

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 PFDN1-HBEGF


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 PFDN1-HBEGF


check button Go to

FGviewer for the breakpoints of chr5:139680001-chr5:139715612

.
- 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
.HBEGF

Q99075

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: Growth factor that mediates its effects via EGFR, ERBB2 and ERBB4. Required for normal cardiac valve formation and normal heart function. Promotes smooth muscle cell proliferation. May be involved in macrophage-mediated cellular proliferation. It is mitogenic for fibroblasts, but not endothelial cells. It is able to bind EGF receptor/EGFR with higher affinity than EGF itself and is a far more potent mitogen for smooth muscle cells than EGF. Also acts as a diphtheria toxin receptor.

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
TgeneHBEGFchr5:139680001chr5:139715612ENST0000023099026185_208132.66666666666666544.3333333333334Topological domainCytoplasmic
TgeneHBEGFchr5:139680001chr5:139715612ENST0000050710427185_208132.66666666666666141.0Topological domainCytoplasmic
TgeneHBEGFchr5:139680001chr5:139715612ENST0000023099026161_184132.66666666666666544.3333333333334TransmembraneHelical
TgeneHBEGFchr5:139680001chr5:139715612ENST0000050710427161_184132.66666666666666141.0TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneHBEGFchr5:139680001chr5:139715612ENST0000023099026104_144132.66666666666666544.3333333333334DomainEGF-like
TgeneHBEGFchr5:139680001chr5:139715612ENST0000050710427104_144132.66666666666666141.0DomainEGF-like
TgeneHBEGFchr5:139680001chr5:139715612ENST000002309902620_160132.66666666666666544.3333333333334Topological domainExtracellular
TgeneHBEGFchr5:139680001chr5:139715612ENST000005071042720_160132.66666666666666141.0Topological domainExtracellular


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Fusion Gene Sequence for PFDN1-HBEGF


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 PFDN1-HBEGF


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 PFDN1-HBEGF


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 PFDN1-HBEGF


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneHBEGFC0014175Endometriosis1CTD_human
TgeneHBEGFC0014549Tonic-Clonic Epilepsy1CTD_human
TgeneHBEGFC0022660Kidney Failure, Acute1CTD_human
TgeneHBEGFC0022661Kidney Failure, Chronic1CTD_human
TgeneHBEGFC0024623Malignant neoplasm of stomach1CTD_human
TgeneHBEGFC0035126Reperfusion Injury1CTD_human
TgeneHBEGFC0038356Stomach Neoplasms1CTD_human
TgeneHBEGFC0087031Juvenile-Onset Still Disease1CTD_human
TgeneHBEGFC0149721Left Ventricular Hypertrophy1CTD_human
TgeneHBEGFC0269102Endometrioma1CTD_human
TgeneHBEGFC0520459Necrotizing Enterocolitis1CTD_human
TgeneHBEGFC0751117Cryptogenic Tonic-Clonic Epilepsy1CTD_human
TgeneHBEGFC0751118Epilepsy, Tonic-Clonic, Familial1CTD_human
TgeneHBEGFC0751119Epilepsy, Tonic-Clonic, Symptomatic1CTD_human
TgeneHBEGFC0876994Cardiotoxicity1CTD_human
TgeneHBEGFC1565662Acute Kidney Insufficiency1CTD_human
TgeneHBEGFC1708349Hereditary Diffuse Gastric Cancer1CTD_human
TgeneHBEGFC2609414Acute kidney injury1CTD_human
TgeneHBEGFC3495559Juvenile arthritis1CTD_human
TgeneHBEGFC3714758Juvenile psoriatic arthritis1CTD_human
TgeneHBEGFC4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
TgeneHBEGFC4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human