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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:SFMBT1-WNT7A

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SFMBT1-WNT7A
FusionPDB ID: 81106
FusionGDB2.0 ID: 81106
HgeneTgene
Gene symbol

SFMBT1

WNT7A

Gene ID

51460

7476

Gene nameScm like with four mbt domains 1Wnt family member 7A
SynonymsRU1|SFMBT|hSFMBTWnt-7a
Cytomap

3p21.1

3p25.1

Type of geneprotein-codingprotein-coding
Descriptionscm-like with four MBT domains protein 1Scm-related gene containing four mbt domainsScm-related gene product containing four mbt domainsrenal ubiquitous protein 1protein Wnt-7aproto-oncogene Wnt7a proteinwingless-type MMTV integration site family, member 7A
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000296295, ENST00000358080, 
ENST00000394750, ENST00000394752, 
ENST00000470575, 
ENST00000497808, 
ENST00000285018, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 15 X 11=29704 X 3 X 4=48
# samples 226
** MAII scorelog2(22/2970*10)=-3.75488750216347
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/48*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SFMBT1 [Title/Abstract] AND WNT7A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SFMBT1(53003117)-WNT7A(13916670), # samples:3
Anticipated loss of major functional domain due to fusion event.SFMBT1-WNT7A 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.
SFMBT1-WNT7A 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.
SFMBT1-WNT7A 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.
SFMBT1-WNT7A 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.
SFMBT1-WNT7A seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
SFMBT1-WNT7A seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SFMBT1-WNT7A 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
HgeneSFMBT1

GO:0045892

negative regulation of transcription, DNA-templated

23592795

TgeneWNT7A

GO:0001502

cartilage condensation

17202865

TgeneWNT7A

GO:0002062

chondrocyte differentiation

17202865

TgeneWNT7A

GO:0021846

cell proliferation in forebrain

12843296

TgeneWNT7A

GO:0032270

positive regulation of cellular protein metabolic process

16805831

TgeneWNT7A

GO:0035313

wound healing, spreading of epidermal cells

15802269

TgeneWNT7A

GO:0045893

positive regulation of transcription, DNA-templated

15802269

TgeneWNT7A

GO:0045944

positive regulation of transcription by RNA polymerase II

12857724

TgeneWNT7A

GO:0048864

stem cell development

12843296

TgeneWNT7A

GO:0050768

negative regulation of neurogenesis

12843296

TgeneWNT7A

GO:0051965

positive regulation of synapse assembly

18986540

TgeneWNT7A

GO:0060054

positive regulation of epithelial cell proliferation involved in wound healing

15802269

TgeneWNT7A

GO:0060070

canonical Wnt signaling pathway

12857724|15802269|16805831|18986540|28733458

TgeneWNT7A

GO:0060071

Wnt signaling pathway, planar cell polarity pathway

15802269

TgeneWNT7A

GO:0060997

dendritic spine morphogenesis

21670302

TgeneWNT7A

GO:1904891

positive regulation of excitatory synapse assembly

21670302

TgeneWNT7A

GO:1905606

regulation of presynapse assembly

20530549

TgeneWNT7A

GO:2000463

positive regulation of excitatory postsynaptic potential

21670302


check buttonFusion gene breakpoints across SFMBT1 (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 WNT7A (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-38-4630-01ASFMBT1chr3

53003117

-WNT7Achr3

13896300

-
ChimerDB4LUADTCGA-38-4630-01ASFMBT1chr3

53003117

-WNT7Achr3

13916670

-


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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)
ENST00000394752SFMBT1chr353003117-ENST00000285018WNT7Achr313896300-38494113441162272
ENST00000296295SFMBT1chr353003117-ENST00000285018WNT7Achr313896300-38353973301148272

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
ENST00000394752ENST00000285018SFMBT1chr353003117-WNT7Achr313896300-0.0016275820.9983725
ENST00000296295ENST00000285018SFMBT1chr353003117-WNT7Achr313896300-0.0016218070.99837816

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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

>81106_81106_1_SFMBT1-WNT7A_SFMBT1_chr3_53003117_ENST00000296295_WNT7A_chr3_13896300_ENST00000285018_length(amino acids)=272AA_BP=19
MFWEDIACLYAVEMNGEQQLDAGSREAAFTYAIIAAGVAHAITAACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFV
DAREIKQNARTLMNLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEPVRASRNKRPTFLKIKKP
LSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYT

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

>81106_81106_2_SFMBT1-WNT7A_SFMBT1_chr3_53003117_ENST00000394752_WNT7A_chr3_13896300_ENST00000285018_length(amino acids)=272AA_BP=19
MFWEDIACLYAVEMNGEQQLDAGSREAAFTYAIIAAGVAHAITAACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFV
DAREIKQNARTLMNLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEPVRASRNKRPTFLKIKKP
LSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYT

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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/chr3:53003117/chr3:13916670)
- 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
TgeneWNT7Achr3:53003117chr3:13896300ENST0000028501814238_26699.33333333333333350.0RegionIntrinsically disordered linker

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000296295-220796_8649.333333333333334824.0DomainNote=SAM
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000358080-322796_8649.333333333333334867.0DomainNote=SAM
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394750-322796_8649.333333333333334867.0DomainNote=SAM
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394752-221796_8649.333333333333334867.0DomainNote=SAM
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000296295-22034_429.333333333333334824.0RegionNote=Antigenic epitope
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000358080-32234_429.333333333333334867.0RegionNote=Antigenic epitope
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394750-32234_429.333333333333334867.0RegionNote=Antigenic epitope
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394752-22134_429.333333333333334867.0RegionNote=Antigenic epitope
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000296295-220128_2329.333333333333334824.0RepeatNote=MBT 2
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000296295-22020_1209.333333333333334824.0RepeatNote=MBT 1
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000296295-220242_3489.333333333333334824.0RepeatNote=MBT 3
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000296295-220356_4539.333333333333334824.0RepeatNote=MBT 4
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000358080-322128_2329.333333333333334867.0RepeatNote=MBT 2
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000358080-32220_1209.333333333333334867.0RepeatNote=MBT 1
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000358080-322242_3489.333333333333334867.0RepeatNote=MBT 3
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000358080-322356_4539.333333333333334867.0RepeatNote=MBT 4
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394750-322128_2329.333333333333334867.0RepeatNote=MBT 2
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394750-32220_1209.333333333333334867.0RepeatNote=MBT 1
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394750-322242_3489.333333333333334867.0RepeatNote=MBT 3
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394750-322356_4539.333333333333334867.0RepeatNote=MBT 4
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394752-221128_2329.333333333333334867.0RepeatNote=MBT 2
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394752-22120_1209.333333333333334867.0RepeatNote=MBT 1
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394752-221242_3489.333333333333334867.0RepeatNote=MBT 3
HgeneSFMBT1chr3:53003117chr3:13896300ENST00000394752-221356_4539.333333333333334867.0RepeatNote=MBT 4


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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
SFMBT1
WNT7A


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 SFMBT1-WNT7A


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 SFMBT1-WNT7A


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