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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:PCMT1-HSP90B1 (FusionGDB2 ID:62955)

Fusion Gene Summary for PCMT1-HSP90B1

check button Fusion gene summary
Fusion gene informationFusion gene name: PCMT1-HSP90B1
Fusion gene ID: 62955
HgeneTgene
Gene symbol

PCMT1

HSP90B1

Gene ID

5110

7184

Gene nameprotein-L-isoaspartate (D-aspartate) O-methyltransferaseheat shock protein 90 beta family member 1
SynonymsPIMTECGP|GP96|GRP94|HEL-S-125m|HEL35|TRA1
Cytomap

6q25.1

12q23.3

Type of geneprotein-codingprotein-coding
Descriptionprotein-L-isoaspartate(D-aspartate) O-methyltransferaseL-isoaspartyl protein carboxyl methyltransferaseepididymis secretory sperm binding proteinprotein L-isoaspartyl/D-aspartyl methyltransferaseprotein-beta-aspartate methyltransferaseendoplasmin94 kDa glucose-regulated proteinendothelial cell (HBMEC) glycoproteinepididymis luminal protein 35epididymis secretory sperm binding protein Li 125mheat shock protein 90 kDa beta member 1heat shock protein 90kDa beta (Grp94), member 1hea
Modification date2020031320200320
UniProtAcc.

P14625

Ensembl transtripts involved in fusion geneENST00000367384, ENST00000367378, 
ENST00000464889, ENST00000367380, 
ENST00000544496, ENST00000480010, 
ENST00000299767, 
Fusion gene scores* DoF score5 X 4 X 4=8021 X 21 X 8=3528
# samples 525
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(25/3528*10)=-3.81885056089543
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PCMT1 [Title/Abstract] AND HSP90B1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPCMT1(150114805)-HSP90B1(104340634), # samples:2
Anticipated loss of major functional domain due to fusion event.PCMT1-HSP90B1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
PCMT1-HSP90B1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PCMT1-HSP90B1 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
TgeneHSP90B1

GO:0001666

response to hypoxia

15620698

TgeneHSP90B1

GO:0031247

actin rod assembly

19000834

TgeneHSP90B1

GO:0043666

regulation of phosphoprotein phosphatase activity

19000834

TgeneHSP90B1

GO:0071318

cellular response to ATP

19000834


check buttonFusion gene breakpoints across PCMT1 (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 HSP90B1 (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
ChimerDB4UCECTCGA-AX-A3G7-01APCMT1chr6

150114805

+HSP90B1chr12

104340634

+
ChimerDB4UCECTCGA-AX-A3G7-01APCMT1chr6

150114805

+HSP90B1chr12

104340634

+


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Fusion Gene ORF analysis for PCMT1-HSP90B1

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-shiftENST00000367384ENST00000299767PCMT1chr6

150114805

+HSP90B1chr12

104340634

+
Frame-shiftENST00000367378ENST00000299767PCMT1chr6

150114805

+HSP90B1chr12

104340634

+
Frame-shiftENST00000464889ENST00000299767PCMT1chr6

150114805

+HSP90B1chr12

104340634

+
Frame-shiftENST00000367380ENST00000299767PCMT1chr6

150114805

+HSP90B1chr12

104340634

+
Frame-shiftENST00000544496ENST00000299767PCMT1chr6

150114805

+HSP90B1chr12

104340634

+
intron-3CDSENST00000480010ENST00000299767PCMT1chr6

150114805

+HSP90B1chr12

104340634

+

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 PCMT1-HSP90B1


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 PCMT1-HSP90B1


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
.HSP90B1

P14625

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: Molecular chaperone that functions in the processing and transport of secreted proteins (By similarity). When associated with CNPY3, required for proper folding of Toll-like receptors (By similarity). Functions in endoplasmic reticulum associated degradation (ERAD) (PubMed:18264092). Has ATPase activity (By similarity). May participate in the unfolding of cytosolic leaderless cargos (lacking the secretion signal sequence) such as the interleukin 1/IL-1 to facilitate their translocation into the ERGIC (endoplasmic reticulum-Golgi intermediate compartment) and secretion; the translocation process is mediated by the cargo receptor TMED10 (PubMed:32272059). {ECO:0000250|UniProtKB:P08113, ECO:0000269|PubMed:18264092, ECO:0000269|PubMed:32272059}.

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 PCMT1-HSP90B1


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 PCMT1-HSP90B1


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 PCMT1-HSP90B1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneHSP90B1P14625DB00615RifabutinOther/unknownSmall moleculeApproved|Investigational
TgeneHSP90B1P14625DB00615RifabutinOther/unknownSmall moleculeApproved|Investigational
TgeneHSP90B1P14625DB00615RifabutinOther/unknownSmall moleculeApproved|Investigational
TgeneHSP90B1P14625DB09130CopperSmall moleculeApproved|Investigational
TgeneHSP90B1P14625DB09130CopperSmall moleculeApproved|Investigational
TgeneHSP90B1P14625DB09130CopperSmall moleculeApproved|Investigational

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Related Diseases for PCMT1-HSP90B1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePCMT1C0038219Status Dysraphicus1CTD_human
HgenePCMT1C0080178Spina Bifida1CTD_human
HgenePCMT1C0266508Rachischisis1CTD_human
TgeneHSP90B1C0005586Bipolar Disorder3PSYGENET
TgeneHSP90B1C0033578Prostatic Neoplasms1CTD_human
TgeneHSP90B1C0376358Malignant neoplasm of prostate1CTD_human