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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:SFRP2-SFRP2 (FusionGDB2 ID:80574)

Fusion Gene Summary for SFRP2-SFRP2

check button Fusion gene summary
Fusion gene informationFusion gene name: SFRP2-SFRP2
Fusion gene ID: 80574
HgeneTgene
Gene symbol

SFRP2

SFRP2

Gene ID

6423

6423

Gene namesecreted frizzled related protein 2secreted frizzled related protein 2
SynonymsFRP-2|SARP1|SDF-5FRP-2|SARP1|SDF-5
Cytomap

4q31.3

4q31.3

Type of geneprotein-codingprotein-coding
Descriptionsecreted frizzled-related protein 2SARP-1sFRP-2secreted apoptosis related protein 1testicular tissue protein Li 170secreted frizzled-related protein 2SARP-1sFRP-2secreted apoptosis related protein 1testicular tissue protein Li 170
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000274063, ENST00000274063, 
Fusion gene scores* DoF score3 X 3 X 1=92 X 2 X 2=8
# samples 32
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: SFRP2 [Title/Abstract] AND SFRP2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSFRP2(154701977)-SFRP2(154702799), # 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
HgeneSFRP2

GO:0008284

positive regulation of cell proliferation

10980594

HgeneSFRP2

GO:0008285

negative regulation of cell proliferation

20208569

HgeneSFRP2

GO:0010719

negative regulation of epithelial to mesenchymal transition

19095296

HgeneSFRP2

GO:0030178

negative regulation of Wnt signaling pathway

20208569

HgeneSFRP2

GO:0030308

negative regulation of cell growth

20208569

HgeneSFRP2

GO:0045600

positive regulation of fat cell differentiation

12055200

HgeneSFRP2

GO:0045892

negative regulation of transcription, DNA-templated

19095296

HgeneSFRP2

GO:0050680

negative regulation of epithelial cell proliferation

19095296

HgeneSFRP2

GO:0090090

negative regulation of canonical Wnt signaling pathway

17471511

TgeneSFRP2

GO:0008284

positive regulation of cell proliferation

10980594

TgeneSFRP2

GO:0008285

negative regulation of cell proliferation

20208569

TgeneSFRP2

GO:0010719

negative regulation of epithelial to mesenchymal transition

19095296

TgeneSFRP2

GO:0030178

negative regulation of Wnt signaling pathway

20208569

TgeneSFRP2

GO:0030308

negative regulation of cell growth

20208569

TgeneSFRP2

GO:0045600

positive regulation of fat cell differentiation

12055200

TgeneSFRP2

GO:0045892

negative regulation of transcription, DNA-templated

19095296

TgeneSFRP2

GO:0050680

negative regulation of epithelial cell proliferation

19095296

TgeneSFRP2

GO:0090090

negative regulation of canonical Wnt signaling pathway

17471511


check buttonFusion gene breakpoints across SFRP2 (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 SFRP2 (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
ChiTaRS5.0N/ACN431023SFRP2chr4

154701977

+SFRP2chr4

154702799

-


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Fusion Gene ORF analysis for SFRP2-SFRP2

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-3CDSENST00000274063ENST00000274063SFRP2chr4

154701977

+SFRP2chr4

154702799

-

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 SFRP2-SFRP2


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 SFRP2-SFRP2


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
..
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: 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.

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 SFRP2-SFRP2


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 SFRP2-SFRP2


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 SFRP2-SFRP2


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 SFRP2-SFRP2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSFRP2C0009402Colorectal Carcinoma2CTD_human
HgeneSFRP2C0009404Colorectal Neoplasms2CTD_human
HgeneSFRP2C0006142Malignant neoplasm of breast1CTD_human
HgeneSFRP2C0007134Renal Cell Carcinoma1CTD_human
HgeneSFRP2C0021390Inflammatory Bowel Diseases1CTD_human
HgeneSFRP2C0279702Conventional (Clear Cell) Renal Cell Carcinoma1CTD_human
HgeneSFRP2C0678222Breast Carcinoma1CTD_human
HgeneSFRP2C1257931Mammary Neoplasms, Human1CTD_human
HgeneSFRP2C1266042Chromophobe Renal Cell Carcinoma1CTD_human
HgeneSFRP2C1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
HgeneSFRP2C1266044Collecting Duct Carcinoma of the Kidney1CTD_human
HgeneSFRP2C1306837Papillary Renal Cell Carcinoma1CTD_human
HgeneSFRP2C1458155Mammary Neoplasms1CTD_human
HgeneSFRP2C4704874Mammary Carcinoma, Human1CTD_human
TgeneSFRP2C0009402Colorectal Carcinoma2CTD_human
TgeneSFRP2C0009404Colorectal Neoplasms2CTD_human
TgeneSFRP2C0006142Malignant neoplasm of breast1CTD_human
TgeneSFRP2C0007134Renal Cell Carcinoma1CTD_human
TgeneSFRP2C0021390Inflammatory Bowel Diseases1CTD_human
TgeneSFRP2C0279702Conventional (Clear Cell) Renal Cell Carcinoma1CTD_human
TgeneSFRP2C0678222Breast Carcinoma1CTD_human
TgeneSFRP2C1257931Mammary Neoplasms, Human1CTD_human
TgeneSFRP2C1266042Chromophobe Renal Cell Carcinoma1CTD_human
TgeneSFRP2C1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
TgeneSFRP2C1266044Collecting Duct Carcinoma of the Kidney1CTD_human
TgeneSFRP2C1306837Papillary Renal Cell Carcinoma1CTD_human
TgeneSFRP2C1458155Mammary Neoplasms1CTD_human
TgeneSFRP2C4704874Mammary Carcinoma, Human1CTD_human