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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 16841

FusionGeneSummary for HSP90AB1_DNAJC21

check button Fusion gene summary
Fusion gene informationFusion gene name: HSP90AB1_DNAJC21
Fusion gene ID: 16841
HgeneTgene
Gene symbol

HSP90AB1

DNAJC21

Gene ID

3326

134218

Gene nameheat shock protein 90 alpha family class B member 1DnaJ heat shock protein family (Hsp40) member C21
SynonymsD6S182|HSP84|HSP90B|HSPC2|HSPCBBMFS3|DNAJA5|GS3|JJJ1
Cytomap

6p21.1

5p13.2

Type of geneprotein-codingprotein-coding
Descriptionheat shock protein HSP 90-betaHSP90-betaheat shock 84 kDaheat shock 90kD protein 1, betaheat shock protein 90 kDaheat shock protein 90kDa alpha (cytosolic), class B member 1heat shock protein 90kDa alpha family class B member 1dnaJ homolog subfamily C member 21DnaJ (Hsp40) homolog, subfamily C, member 21DnaJ homology subfamily A member 5JJJ1 DnaJ domain protein homologdnaJ homolog subfamily A member 5
Modification date2018052220180519
UniProtAcc

P08238

Q5F1R6

Ensembl transtripts involved in fusion geneENST00000353801, ENST00000371646, 
ENST00000371554, 
ENST00000342382, 
ENST00000303525, ENST00000382021, 
ENST00000512136, 
Fusion gene scores* DoF score6 X 5 X 3=902 X 2 X 2=8
# samples 62
** MAII scorelog2(6/90*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: HSP90AB1 [Title/Abstract] AND DNAJC21 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneHSP90AB1

GO:0007004

telomere maintenance via telomerase

10197982

HgeneHSP90AB1

GO:0030511

positive regulation of transforming growth factor beta receptor signaling pathway

24613385

HgeneHSP90AB1

GO:0031396

regulation of protein ubiquitination

16809764

HgeneHSP90AB1

GO:0032435

negative regulation of proteasomal ubiquitin-dependent protein catabolic process

24613385

HgeneHSP90AB1

GO:0032516

positive regulation of phosphoprotein phosphatase activity

26593036

HgeneHSP90AB1

GO:0051131

chaperone-mediated protein complex assembly

10811660

HgeneHSP90AB1

GO:0051973

positive regulation of telomerase activity

10197982

HgeneHSP90AB1

GO:1901389

negative regulation of transforming growth factor beta activation

20599762

HgeneHSP90AB1

GO:1905323

telomerase holoenzyme complex assembly

10197982

HgeneHSP90AB1

GO:2000010

positive regulation of protein localization to cell surface

23431407


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1BM750525HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-shiftENST00000353801ENST00000342382HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
Frame-shiftENST00000353801ENST00000303525HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
Frame-shiftENST00000353801ENST00000382021HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
5CDS-intronENST00000353801ENST00000512136HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
Frame-shiftENST00000371646ENST00000342382HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
Frame-shiftENST00000371646ENST00000303525HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
Frame-shiftENST00000371646ENST00000382021HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
5CDS-intronENST00000371646ENST00000512136HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
Frame-shiftENST00000371554ENST00000342382HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
Frame-shiftENST00000371554ENST00000303525HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
Frame-shiftENST00000371554ENST00000382021HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+
5CDS-intronENST00000371554ENST00000512136HSP90AB1chr6

44218221

+DNAJC21chr5

34939013

+

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FusionProtFeatures for HSP90AB1_DNAJC21


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
HSP90AB1

P08238

DNAJC21

Q5F1R6

Molecular chaperone that promotes the maturation,structural maintenance and proper regulation of specific targetproteins involved for instance in cell cycle control and signaltransduction. Undergoes a functional cycle that is linked to itsATPase activity. This cycle probably induces conformationalchanges in the client proteins, thereby causing their activation.Interacts dynamically with various co-chaperones that modulate itssubstrate recognition, ATPase cycle and chaperone function(PubMed:16478993, PubMed:19696785). Engages with a range of clientprotein classes via its interaction with various co-chaperoneproteins or complexes, that act as adapters, simultaneously ableto interact with the specific client and the central chaperoneitself. Recruitment of ATP and co-chaperone followed by clientprotein forms a functional chaperone. After the completion of thechaperoning process, properly folded client protein and co-chaperone leave HSP90 in an ADP-bound partially open conformationand finally, ADP is released from HSP90 which acquires an openconformation for the next cycle (PubMed:27295069,PubMed:26991466). Apart from its chaperone activity, it also playsa role in the regulation of the transcription machinery. HSP90 andits co-chaperones modulate transcription at least at threedifferent levels. In the first place, they alter the steady-statelevels of certain transcription factors in response to variousphysiological cues. Second, they modulate the activity of certainepigenetic modifiers, such as histone deacetylases or DNA methyltransferases, and thereby respond to the change in theenvironment. Third, they participate in the eviction of histonesfrom the promoter region of certain genes and thereby turn on geneexpression (PubMed:25973397). Antagonizes STUB1-mediatedinhibition of TGF-beta signaling via inhibition of STUB1-mediatedSMAD3 ubiquitination and degradation (PubMed:24613385). Promotescell differentiation by chaperoning BIRC2 and thereby protectingfrom auto-ubiquitination and degradation by the proteasomalmachinery (PubMed:18239673). Main chaperone that is involved inthe phosphorylation/activation of the STAT1 by chaperoning bothJAK2 and PRKCE under heat shock and in turn, activates its owntranscription (PubMed:20353823). {ECO:0000269|PubMed:16478993,ECO:0000269|PubMed:18239673, ECO:0000269|PubMed:19696785,ECO:0000269|PubMed:20353823, ECO:0000269|PubMed:24613385,ECO:0000303|PubMed:25973397, ECO:0000303|PubMed:26991466,ECO:0000303|PubMed:27295069}. May act as a co-chaperone for HSP70. May play a role inribosomal RNA (rRNA) biogenesis, possibly in the maturation of the60S subunit. Binds the precursor 45S rRNA.{ECO:0000269|PubMed:27346687}.

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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FusionGeneSequence for HSP90AB1_DNAJC21


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for HSP90AB1_DNAJC21


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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RelatedDrugs for HSP90AB1_DNAJC21


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for HSP90AB1_DNAJC21


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneHSP90AB1C0019693HIV Infections1CTD_human
HgeneHSP90AB1C0033578Prostatic Neoplasms1CTD_human