FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:SPARC-HSP90B1 (FusionGDB2 ID:84907)

Fusion Gene Summary for SPARC-HSP90B1

check button Fusion gene summary
Fusion gene informationFusion gene name: SPARC-HSP90B1
Fusion gene ID: 84907
HgeneTgene
Gene symbol

SPARC

HSP90B1

Gene ID

6678

7184

Gene namesecreted protein acidic and cysteine richheat shock protein 90 beta family member 1
SynonymsBM-40|OI17|ON|ONTECGP|GP96|GRP94|HEL-S-125m|HEL35|TRA1
Cytomap

5q33.1

12q23.3

Type of geneprotein-codingprotein-coding
DescriptionSPARCbasement-membrane protein 40secreted protein, acidic, cysteine-rich (osteonectin)endoplasmin94 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 date2020032920200320
UniProtAcc

SPARC

P14625

Ensembl transtripts involved in fusion geneENST00000231061, ENST00000537849, 
ENST00000299767, 
Fusion gene scores* DoF score39 X 30 X 11=1287021 X 21 X 8=3528
# samples 4725
** MAII scorelog2(47/12870*10)=-4.77520748654306
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: SPARC [Title/Abstract] AND HSP90B1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSPARC(151054173)-HSP90B1(104341152), # samples:1
Anticipated loss of major functional domain due to fusion event.SPARC-HSP90B1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
SPARC-HSP90B1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
SPARC-HSP90B1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
SPARC-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
HgeneSPARC

GO:0001937

negative regulation of endothelial cell proliferation

12867428

HgeneSPARC

GO:0010595

positive regulation of endothelial cell migration

12867428

HgeneSPARC

GO:0016525

negative regulation of angiogenesis

12867428

HgeneSPARC

GO:0022604

regulation of cell morphogenesis

15389586

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 SPARC (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
ChimerDB4READTCGA-AH-6549-01ASPARCchr5

151054173

-HSP90B1chr12

104341152

+


Top

Fusion Gene ORF analysis for SPARC-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-shiftENST00000231061ENST00000299767SPARCchr5

151054173

-HSP90B1chr12

104341152

+
intron-3CDSENST00000537849ENST00000299767SPARCchr5

151054173

-HSP90B1chr12

104341152

+

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

Top

Fusion Genomic Features for SPARC-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.

Top

Fusion Protein Features for SPARC-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
SPARC

SPARC

HSP90B1

P14625

664FUNCTION: 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


Top

Fusion Gene Sequence for SPARC-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.

Top

Fusion Gene PPI Analysis for SPARC-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


Top

Related Drugs for SPARC-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

Top

Related Diseases for SPARC-HSP90B1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSPARCC0023893Liver Cirrhosis, Experimental2CTD_human
HgeneSPARCC0029434Osteogenesis Imperfecta2CTD_human;GENOMICS_ENGLAND
HgeneSPARCC0007102Malignant tumor of colon1CTD_human
HgeneSPARCC0009375Colonic Neoplasms1CTD_human
HgeneSPARCC0009402Colorectal Carcinoma1CTD_human
HgeneSPARCC0009404Colorectal Neoplasms1CTD_human
HgeneSPARCC0019158Hepatitis1CTD_human
HgeneSPARCC0020429Hyperalgesia1CTD_human
HgeneSPARCC0022658Kidney Diseases1CTD_human
HgeneSPARCC0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneSPARCC0023890Liver Cirrhosis1CTD_human
HgeneSPARCC0023931Lobstein Disease1CTD_human
HgeneSPARCC0024031Low Back Pain1CTD_human
HgeneSPARCC0026764Multiple Myeloma1CTD_human
HgeneSPARCC0026998Acute Myeloid Leukemia, M11CTD_human
HgeneSPARCC0027540Necrosis1CTD_human
HgeneSPARCC0027659Neoplasms, Experimental1CTD_human
HgeneSPARCC0040034Thrombocytopenia1CTD_human
HgeneSPARCC0041948Uremia1CTD_human
HgeneSPARCC0043094Weight Gain1CTD_human
HgeneSPARCC0151744Myocardial Ischemia1CTD_human
HgeneSPARCC0158266Intervertebral Disc Degeneration1CTD_human
HgeneSPARCC0206686Adrenocortical carcinoma1CTD_human
HgeneSPARCC0239946Fibrosis, Liver1CTD_human
HgeneSPARCC0268363Osteogenesis imperfecta type IV (disorder)1ORPHANET
HgeneSPARCC0423682Low Back Pain, Mechanical1CTD_human
HgeneSPARCC0423689Low Back Pain, Posterior Compartment1CTD_human
HgeneSPARCC0458247Allodynia1CTD_human
HgeneSPARCC0577660Low Back Pain, Postural1CTD_human
HgeneSPARCC0751211Hyperalgesia, Primary1CTD_human
HgeneSPARCC0751212Hyperalgesia, Secondary1CTD_human
HgeneSPARCC0751213Tactile Allodynia1CTD_human
HgeneSPARCC0751214Hyperalgesia, Thermal1CTD_human
HgeneSPARCC0751648Recurrent Low Back Pain1CTD_human
HgeneSPARCC0919267ovarian neoplasm1CTD_human
HgeneSPARCC1140680Malignant neoplasm of ovary1CTD_human
HgeneSPARCC1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
HgeneSPARCC2717759Degenerative Intervertebral Discs1CTD_human
HgeneSPARCC2936719Mechanical Allodynia1CTD_human
HgeneSPARCC4225301OSTEOGENESIS IMPERFECTA, TYPE XVII1CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneHSP90B1C0005586Bipolar Disorder3PSYGENET
TgeneHSP90B1C0033578Prostatic Neoplasms1CTD_human
TgeneHSP90B1C0376358Malignant neoplasm of prostate1CTD_human