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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:SPARC-ELK3 (FusionGDB2 ID:84902)

Fusion Gene Summary for SPARC-ELK3

check button Fusion gene summary
Fusion gene informationFusion gene name: SPARC-ELK3
Fusion gene ID: 84902
HgeneTgene
Gene symbol

SPARC

ELK3

Gene ID

6678

2004

Gene namesecreted protein acidic and cysteine richETS transcription factor ELK3
SynonymsBM-40|OI17|ON|ONTERP|NET|SAP-2|SAP2
Cytomap

5q33.1

12q23.1

Type of geneprotein-codingprotein-coding
DescriptionSPARCbasement-membrane protein 40secreted protein, acidic, cysteine-rich (osteonectin)ETS domain-containing protein Elk-3ELK3, ETS transcription factorELK3, ETS-domain protein (SRF accessory protein 2)ETS-related protein ERPETS-related protein NETSRF accessory protein 2serum response factor accessory protein 2
Modification date2020032920200313
UniProtAcc

SPARC

P41970

Ensembl transtripts involved in fusion geneENST00000231061, ENST00000537849, 
ENST00000228741, ENST00000552142, 
ENST00000549529, 
Fusion gene scores* DoF score39 X 30 X 11=1287024 X 8 X 11=2112
# samples 4722
** MAII scorelog2(47/12870*10)=-4.77520748654306
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(22/2112*10)=-3.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SPARC [Title/Abstract] AND ELK3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSPARC(151042567)-ELK3(96640958), # samples:5
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
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

TgeneELK3

GO:0045892

negative regulation of transcription, DNA-templated

12933792

TgeneELK3

GO:0045944

positive regulation of transcription by RNA polymerase II

12788937


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 ELK3 (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
ChimerDB4BRCATCGA-BH-A0AZ-01ASPARCchr5

151042567

-ELK3chr12

96640958

+
ChimerDB4KIRCTCGA-BP-4961-01ASPARCchr5

151042567

-ELK3chr12

96640958

+
ChimerDB4SARCTCGA-DX-A3LT-01ASPARCchr5

151042567

-ELK3chr12

96640958

+
ChimerDB4SARCTCGA-DX-A1L3-01ASPARCchr5

151042567

-ELK3chr12

96640958

+
ChimerDB4SKCMTCGA-EB-A6QZ-01ASPARCchr5

151042567

-ELK3chr12

96640958

+


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Fusion Gene ORF analysis for SPARC-ELK3

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
intron-3CDSENST00000231061ENST00000228741SPARCchr5

151042567

-ELK3chr12

96640958

+
intron-intronENST00000231061ENST00000552142SPARCchr5

151042567

-ELK3chr12

96640958

+
intron-intronENST00000231061ENST00000549529SPARCchr5

151042567

-ELK3chr12

96640958

+
intron-3CDSENST00000537849ENST00000228741SPARCchr5

151042567

-ELK3chr12

96640958

+
intron-intronENST00000537849ENST00000552142SPARCchr5

151042567

-ELK3chr12

96640958

+
intron-intronENST00000537849ENST00000549529SPARCchr5

151042567

-ELK3chr12

96640958

+

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 SPARC-ELK3


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 SPARC-ELK3


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

ELK3

P41970

664FUNCTION: May be a negative regulator of transcription, but can activate transcription when coexpressed with Ras, Src or Mos. Forms a ternary complex with the serum response factor and the ETS and SRF motifs of the Fos serum response element.

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 SPARC-ELK3


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 SPARC-ELK3


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 SPARC-ELK3


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 SPARC-ELK3


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
TgeneELK3C0006142Malignant neoplasm of breast1CTD_human
TgeneELK3C0678222Breast Carcinoma1CTD_human
TgeneELK3C1135196Heart Failure, Diastolic1CTD_human
TgeneELK3C1257931Mammary Neoplasms, Human1CTD_human
TgeneELK3C1458155Mammary Neoplasms1CTD_human
TgeneELK3C4704874Mammary Carcinoma, Human1CTD_human