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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:RNF170-SFRP1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RNF170-SFRP1
FusionPDB ID: 74895
FusionGDB2.0 ID: 74895
HgeneTgene
Gene symbol

RNF170

SFRP1

Gene ID

81790

6422

Gene namering finger protein 170secreted frizzled related protein 1
SynonymsADSA|SNAX1FRP|FRP-1|FRP1|FrzA|SARP2
Cytomap

8p11.21

8p11.21

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase RNF170RING-type E3 ubiquitin transferase RNF170putative LAG1-interacting proteinsecreted frizzled-related protein 1SARP-2frizzled-related proteinsFRP-1secreted apoptosis-related protein 2
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000319073, ENST00000319104, 
ENST00000527424, ENST00000534961, 
ENST00000526349, 
ENST00000220772, 
ENST00000379845, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 6 X 6=3244 X 5 X 4=80
# samples 105
** MAII scorelog2(10/324*10)=-1.6959938131099
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RNF170 [Title/Abstract] AND SFRP1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RNF170(42742871)-SFRP1(41123008), # samples:3
Anticipated loss of major functional domain due to fusion event.RNF170-SFRP1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RNF170-SFRP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
RNF170-SFRP1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
TgeneSFRP1

GO:0002244

hematopoietic progenitor cell differentiation

19778523

TgeneSFRP1

GO:0008284

positive regulation of cell proliferation

10980594

TgeneSFRP1

GO:0008285

negative regulation of cell proliferation

10347172|17443492|17994217|19277043|20208569

TgeneSFRP1

GO:0009950

dorsal/ventral axis specification

9192640

TgeneSFRP1

GO:0010629

negative regulation of gene expression

10980594

TgeneSFRP1

GO:0010719

negative regulation of epithelial to mesenchymal transition

19095296

TgeneSFRP1

GO:0014070

response to organic cyclic compound

20208569

TgeneSFRP1

GO:0030177

positive regulation of Wnt signaling pathway

10660608

TgeneSFRP1

GO:0030178

negative regulation of Wnt signaling pathway

9192640|10660608|17500071|20208569

TgeneSFRP1

GO:0030279

negative regulation of ossification

15677765

TgeneSFRP1

GO:0030307

positive regulation of cell growth

10980594|16288033

TgeneSFRP1

GO:0030308

negative regulation of cell growth

19569235|20208569

TgeneSFRP1

GO:0030336

negative regulation of cell migration

10980594

TgeneSFRP1

GO:0042493

response to drug

19072540|19254787

TgeneSFRP1

GO:0043065

positive regulation of apoptotic process

9391078|15677765

TgeneSFRP1

GO:0044344

cellular response to fibroblast growth factor stimulus

17500071

TgeneSFRP1

GO:0045600

positive regulation of fat cell differentiation

12055200|15886250

TgeneSFRP1

GO:0045892

negative regulation of transcription, DNA-templated

10660608|19095296|19277043|20234818

TgeneSFRP1

GO:0045893

positive regulation of transcription, DNA-templated

10660608|15886250|19569235

TgeneSFRP1

GO:0046676

negative regulation of insulin secretion

17994217

TgeneSFRP1

GO:0048147

negative regulation of fibroblast proliferation

19734317

TgeneSFRP1

GO:0050680

negative regulation of epithelial cell proliferation

19095296

TgeneSFRP1

GO:0050732

negative regulation of peptidyl-tyrosine phosphorylation

10980594

TgeneSFRP1

GO:0060070

canonical Wnt signaling pathway

18787224

TgeneSFRP1

GO:0060218

hematopoietic stem cell differentiation

19778523

TgeneSFRP1

GO:0060766

negative regulation of androgen receptor signaling pathway

19277043

TgeneSFRP1

GO:0071356

cellular response to tumor necrosis factor

9391078

TgeneSFRP1

GO:0071363

cellular response to growth factor stimulus

17500071

TgeneSFRP1

GO:0071391

cellular response to estrogen stimulus

18941195

TgeneSFRP1

GO:0071504

cellular response to heparin

17500071

TgeneSFRP1

GO:0090090

negative regulation of canonical Wnt signaling pathway

9391078|10347172|16149051|16288033|17443492|17471511|19095296|19277043|19569235

TgeneSFRP1

GO:0090263

positive regulation of canonical Wnt signaling pathway

18941195

TgeneSFRP1

GO:1902043

positive regulation of extrinsic apoptotic signaling pathway via death domain receptors

9391078

TgeneSFRP1

GO:2000052

positive regulation of non-canonical Wnt signaling pathway

19569235

TgeneSFRP1

GO:2000054

negative regulation of Wnt signaling pathway involved in dorsal/ventral axis specification

9192640

TgeneSFRP1

GO:2000080

negative regulation of canonical Wnt signaling pathway involved in controlling type B pancreatic cell proliferation

17994217

TgeneSFRP1

GO:2000270

negative regulation of fibroblast apoptotic process

14581477

TgeneSFRP1

GO:2000271

positive regulation of fibroblast apoptotic process

14581477


check buttonFusion gene breakpoints across RNF170 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across SFRP1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4LUADTCGA-50-6673-01ARNF170chr8

42742871

-SFRP1chr8

41123008

-
ChimerDB4LUADTCGA-50-6673RNF170chr8

42742870

-SFRP1chr8

41123008

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000319104RNF170chr842742871-ENST00000220772SFRP1chr841123008-377424613387124
ENST00000534961RNF170chr842742871-ENST00000379845SFRP1chr841123008-41406145030168
ENST00000527424RNF170chr842742871-ENST00000220772SFRP1chr841123008-391038241523160
ENST00000319104RNF170chr842742870-ENST00000220772SFRP1chr841123008-377424613387124
ENST00000534961RNF170chr842742870-ENST00000379845SFRP1chr841123008-41406145030168
ENST00000527424RNF170chr842742870-ENST00000220772SFRP1chr841123008-391038241523160

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
ENST00000319104ENST00000220772RNF170chr842742871-SFRP1chr841123008-0.0322876420.9677124
ENST00000534961ENST00000379845RNF170chr842742871-SFRP1chr841123008-0.0433608220.9566392
ENST00000527424ENST00000220772RNF170chr842742871-SFRP1chr841123008-0.032795170.9672048
ENST00000319104ENST00000220772RNF170chr842742870-SFRP1chr841123008-0.0322876420.9677124
ENST00000534961ENST00000379845RNF170chr842742870-SFRP1chr841123008-0.0433608220.9566392
ENST00000527424ENST00000220772RNF170chr842742870-SFRP1chr841123008-0.032795170.9672048

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>74895_74895_1_RNF170-SFRP1_RNF170_chr8_42742870_ENST00000319104_SFRP1_chr8_41123008_ENST00000220772_length(amino acids)=124AA_BP=77
MPGRGGGSGPGNNLSSVAGNWRGSSFAVERPGMAKYQGEVQSLKLDDDSVIEGVSDQVLVAVVVSFALIATLVYALFSTEDENKRSEKRK

--------------------------------------------------------------

>74895_74895_2_RNF170-SFRP1_RNF170_chr8_42742870_ENST00000527424_SFRP1_chr8_41123008_ENST00000220772_length(amino acids)=160AA_BP=113
MRRRVLLRRPVAPSRKLGSARAPAPALQIRKGTSSGLPGRGGGSGPGNNLSSVAGNWRGSSFAVERPGMAKYQGEVQSLKLDDDSVIEGV

--------------------------------------------------------------

>74895_74895_3_RNF170-SFRP1_RNF170_chr8_42742870_ENST00000534961_SFRP1_chr8_41123008_ENST00000379845_length(amino acids)=168AA_BP=
MNFTLIFGHSRSRAALRVGPSTVAGDSGQPRGDSGASRRGRGPGGRRRRLPPPRRASAARATPRRPDPAVRGSAGPDRVGVAAARRTYLS

--------------------------------------------------------------

>74895_74895_4_RNF170-SFRP1_RNF170_chr8_42742871_ENST00000319104_SFRP1_chr8_41123008_ENST00000220772_length(amino acids)=124AA_BP=77
MPGRGGGSGPGNNLSSVAGNWRGSSFAVERPGMAKYQGEVQSLKLDDDSVIEGVSDQVLVAVVVSFALIATLVYALFSTEDENKRSEKRK

--------------------------------------------------------------

>74895_74895_5_RNF170-SFRP1_RNF170_chr8_42742871_ENST00000527424_SFRP1_chr8_41123008_ENST00000220772_length(amino acids)=160AA_BP=113
MRRRVLLRRPVAPSRKLGSARAPAPALQIRKGTSSGLPGRGGGSGPGNNLSSVAGNWRGSSFAVERPGMAKYQGEVQSLKLDDDSVIEGV

--------------------------------------------------------------

>74895_74895_6_RNF170-SFRP1_RNF170_chr8_42742871_ENST00000534961_SFRP1_chr8_41123008_ENST00000379845_length(amino acids)=168AA_BP=
MNFTLIFGHSRSRAALRVGPSTVAGDSGQPRGDSGASRRGRGPGGRRRRLPPPRRASAARATPRRPDPAVRGSAGPDRVGVAAARRTYLS

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr8:42742871/chr8:41123008)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRNF170chr8:42742870chr8:41123008ENST00000319104-261_2445.666666666666664201.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000527424-271_2445.666666666666664259.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000534961-271_2445.666666666666664259.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000319104-261_2445.666666666666664201.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000527424-271_2445.666666666666664259.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000534961-271_2445.666666666666664259.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000319104-2625_4545.666666666666664201.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000527424-2725_4545.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000534961-2725_4545.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000319104-2625_4545.666666666666664201.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000527424-2725_4545.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000534961-2725_4545.666666666666664259.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRNF170chr8:42742870chr8:41123008ENST00000319073-261_240163.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000319073-26223_2230163.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000319073-26245_2580163.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000319073-2646_2010163.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000319104-26223_22345.666666666666664201.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000319104-26245_25845.666666666666664201.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000319104-2646_20145.666666666666664201.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000526349-171_240175.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000526349-17223_2230175.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000526349-17245_2580175.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000526349-1746_2010175.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000527424-27223_22345.666666666666664259.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000527424-27245_25845.666666666666664259.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000527424-2746_20145.666666666666664259.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000534961-27223_22345.666666666666664259.0Topological domainLumenal
HgeneRNF170chr8:42742870chr8:41123008ENST00000534961-27245_25845.666666666666664259.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000534961-2746_20145.666666666666664259.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000319073-261_240163.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000319073-26223_2230163.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000319073-26245_2580163.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000319073-2646_2010163.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000319104-26223_22345.666666666666664201.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000319104-26245_25845.666666666666664201.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000319104-2646_20145.666666666666664201.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000526349-171_240175.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000526349-17223_2230175.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000526349-17245_2580175.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000526349-1746_2010175.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000527424-27223_22345.666666666666664259.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000527424-27245_25845.666666666666664259.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000527424-2746_20145.666666666666664259.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000534961-27223_22345.666666666666664259.0Topological domainLumenal
HgeneRNF170chr8:42742871chr8:41123008ENST00000534961-27245_25845.666666666666664259.0Topological domainCytoplasmic
HgeneRNF170chr8:42742871chr8:41123008ENST00000534961-2746_20145.666666666666664259.0Topological domainCytoplasmic
HgeneRNF170chr8:42742870chr8:41123008ENST00000319073-26202_2220163.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000319073-26224_2440163.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000319073-2625_450163.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000319104-26202_22245.666666666666664201.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000319104-26224_24445.666666666666664201.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000526349-17202_2220175.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000526349-17224_2440175.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000526349-1725_450175.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000527424-27202_22245.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000527424-27224_24445.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000534961-27202_22245.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000534961-27224_24445.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000319073-26202_2220163.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000319073-26224_2440163.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000319073-2625_450163.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000319104-26202_22245.666666666666664201.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000319104-26224_24445.666666666666664201.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000526349-17202_2220175.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000526349-17224_2440175.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000526349-1725_450175.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000527424-27202_22245.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000527424-27224_24445.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000534961-27202_22245.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742871chr8:41123008ENST00000534961-27224_24445.666666666666664259.0TransmembraneHelical
HgeneRNF170chr8:42742870chr8:41123008ENST00000319073-2687_1300163.0Zinc fingerRING-type
HgeneRNF170chr8:42742870chr8:41123008ENST00000319104-2687_13045.666666666666664201.0Zinc fingerRING-type
HgeneRNF170chr8:42742870chr8:41123008ENST00000526349-1787_1300175.0Zinc fingerRING-type
HgeneRNF170chr8:42742870chr8:41123008ENST00000527424-2787_13045.666666666666664259.0Zinc fingerRING-type
HgeneRNF170chr8:42742870chr8:41123008ENST00000534961-2787_13045.666666666666664259.0Zinc fingerRING-type
HgeneRNF170chr8:42742871chr8:41123008ENST00000319073-2687_1300163.0Zinc fingerRING-type
HgeneRNF170chr8:42742871chr8:41123008ENST00000319104-2687_13045.666666666666664201.0Zinc fingerRING-type
HgeneRNF170chr8:42742871chr8:41123008ENST00000526349-1787_1300175.0Zinc fingerRING-type
HgeneRNF170chr8:42742871chr8:41123008ENST00000527424-2787_13045.666666666666664259.0Zinc fingerRING-type
HgeneRNF170chr8:42742871chr8:41123008ENST00000534961-2787_13045.666666666666664259.0Zinc fingerRING-type
TgeneSFRP1chr8:42742870chr8:41123008ENST0000022077213186_306207.33333333333334315.0DomainNTR
TgeneSFRP1chr8:42742870chr8:41123008ENST000002207721353_169207.33333333333334315.0DomainFZ
TgeneSFRP1chr8:42742871chr8:41123008ENST0000022077213186_306207.33333333333334315.0DomainNTR
TgeneSFRP1chr8:42742871chr8:41123008ENST000002207721353_169207.33333333333334315.0DomainFZ


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
RNF170
SFRP1


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to RNF170-SFRP1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to RNF170-SFRP1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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