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Center for Computational Systems Medicine level2
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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 Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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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:SMAD7-DYM

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SMAD7-DYM
FusionPDB ID: 83829
FusionGDB2.0 ID: 83829
HgeneTgene
Gene symbol

SMAD7

DYM

Gene ID

4092

54808

Gene nameSMAD family member 7dymeclin
SynonymsCRCS3|MADH7|MADH8DMC|SMC
Cytomap

18q21.1

18q21.1

Type of geneprotein-codingprotein-coding
Descriptionmothers against decapentaplegic homolog 7MAD (mothers against decapentaplegic, Drosophila) homolog 7MAD homolog 8Mothers against decapentaplegic, drosophila, homolog of, 7SMAD, mothers against DPP homolog 7hSMAD7mothers against DPP homolog 8dymeclindyggve-Melchior-Clausen syndrome protein
Modification date2020032020200313
UniProtAcc.

Q7RTS9

Ensembl transtripts involved in fusion geneENST idsENST00000262158, ENST00000589634, 
ENST00000591805, ENST00000585986, 
ENST00000578396, ENST00000584977, 
ENST00000269445, ENST00000442713, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 4 X 5=8019 X 11 X 13=2717
# samples 624
** MAII scorelog2(6/80*10)=-0.415037499278844
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(24/2717*10)=-3.50090825461346
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SMAD7 [Title/Abstract] AND DYM [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SMAD7(46468851)-DYM(46645296), # samples:2
SMAD7(46468851)-DYM(46570574), # samples:2
Anticipated loss of major functional domain due to fusion event.SMAD7-DYM 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.
SMAD7-DYM 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.
SMAD7-DYM 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.
SMAD7-DYM 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.
SMAD7-DYM seems lost the major protein functional domain in Hgene partner, which is a essential gene 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
HgeneSMAD7

GO:0000122

negative regulation of transcription by RNA polymerase II

17438144

HgeneSMAD7

GO:0010801

negative regulation of peptidyl-threonine phosphorylation

18593713

HgeneSMAD7

GO:0010944

negative regulation of transcription by competitive promoter binding

17438144

HgeneSMAD7

GO:0022409

positive regulation of cell-cell adhesion

18593713

HgeneSMAD7

GO:0030512

negative regulation of transforming growth factor beta receptor signaling pathway

12151385|17438144|18762808

HgeneSMAD7

GO:0030514

negative regulation of BMP signaling pathway

17438144

HgeneSMAD7

GO:0031397

negative regulation of protein ubiquitination

18593713

HgeneSMAD7

GO:0031398

positive regulation of protein ubiquitination

16720724

HgeneSMAD7

GO:0032436

positive regulation of proteasomal ubiquitin-dependent protein catabolic process

11278251

HgeneSMAD7

GO:0032925

regulation of activin receptor signaling pathway

16720724

HgeneSMAD7

GO:0033137

negative regulation of peptidyl-serine phosphorylation

18593713

HgeneSMAD7

GO:0034629

cellular protein-containing complex localization

18593713

HgeneSMAD7

GO:0043433

negative regulation of DNA-binding transcription factor activity

17438144

HgeneSMAD7

GO:0050821

protein stabilization

18593713

HgeneSMAD7

GO:0051444

negative regulation of ubiquitin-protein transferase activity

18593713

HgeneSMAD7

GO:0060394

negative regulation of pathway-restricted SMAD protein phosphorylation

17438144


check buttonFusion gene breakpoints across SMAD7 (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 DYM (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
ChimerDB4BRCATCGA-BH-A1FD-01ASMAD7chr18

46468851

-DYMchr18

46690157

-
ChimerDB4LIHCTCGA-DD-A73F-01ASMAD7chr18

46468851

-DYMchr18

46645296

-
ChimerDB4UCSTCGA-NA-A4R0-01ASMAD7chr18

46468851

-DYMchr18

46570574

-
ChimerDB4UCSTCGA-NA-A4ROSMAD7chr18

46468851

-DYMchr18

46570574

-


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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)
ENST00000591805SMAD7chr1846468851-ENST00000442713DYMchr1846570574-770234101493130
ENST00000591805SMAD7chr1846468851-ENST00000442713DYMchr1846690157-1170234244783179
ENST00000591805SMAD7chr1846468851-ENST00000269445DYMchr1846690157-1019234244783179

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
ENST00000591805ENST00000442713SMAD7chr1846468851-DYMchr1846570574-0.149589970.85041004
ENST00000591805ENST00000442713SMAD7chr1846468851-DYMchr1846690157-0.0063795380.99362046
ENST00000591805ENST00000269445SMAD7chr1846468851-DYMchr1846690157-0.0099967940.9900032

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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

>83829_83829_1_SMAD7-DYM_SMAD7_chr18_46468851_ENST00000591805_DYM_chr18_46570574_ENST00000442713_length(amino acids)=130AA_BP=44
MESPPPPYSRYPMDFLKPTADCPDAVPSSAETGGTNYLAPGGLSEISRIEIQICGRGAARGVFYPLCLVSCLQLSSRPVLESTGHPAVHH

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

>83829_83829_2_SMAD7-DYM_SMAD7_chr18_46468851_ENST00000591805_DYM_chr18_46690157_ENST00000269445_length(amino acids)=179AA_BP=
MLSKKHNKVLEQATQSLRGSLSSNDVPLPDYAQDLNVIEEVIRMMLEIINSCLTNSLHHNPNLVYALLYKRDLFEQFRTHPSFQDIMQNI

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

>83829_83829_3_SMAD7-DYM_SMAD7_chr18_46468851_ENST00000591805_DYM_chr18_46690157_ENST00000442713_length(amino acids)=179AA_BP=
MLSKKHNKVLEQATQSLRGSLSSNDVPLPDYAQDLNVIEEVIRMMLEIINSCLTNSLHHNPNLVYALLYKRDLFEQFRTHPSFQDIMQNI

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

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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/chr18:46468851/chr18:46645296)
- 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
.DYM

Q7RTS9

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: Necessary for correct organization of Golgi apparatus. Involved in bone development. {ECO:0000269|PubMed:21280149}.

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
HgeneSMAD7chr18:46468851chr18:46570574ENST00000262158-34207_210247.33333333333334427.0Compositional biasNote=Poly-Pro
HgeneSMAD7chr18:46468851chr18:46570574ENST00000262158-3427_35247.33333333333334427.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46570574ENST00000262158-3449_56247.33333333333334427.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46570574ENST00000589634-34207_210246.33333333333334426.0Compositional biasNote=Poly-Pro
HgeneSMAD7chr18:46468851chr18:46570574ENST00000589634-3427_35246.33333333333334426.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46570574ENST00000589634-3449_56246.33333333333334426.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46570574ENST00000591805-3427_3532.333333333333336212.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46690157ENST00000262158-34207_210247.33333333333334427.0Compositional biasNote=Poly-Pro
HgeneSMAD7chr18:46468851chr18:46690157ENST00000262158-3427_35247.33333333333334427.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46690157ENST00000262158-3449_56247.33333333333334427.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46690157ENST00000589634-34207_210246.33333333333334426.0Compositional biasNote=Poly-Pro
HgeneSMAD7chr18:46468851chr18:46690157ENST00000589634-3427_35246.33333333333334426.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46690157ENST00000589634-3449_56246.33333333333334426.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46690157ENST00000591805-3427_3532.333333333333336212.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46570574ENST00000262158-3464_207247.33333333333334427.0DomainMH1
HgeneSMAD7chr18:46468851chr18:46570574ENST00000589634-3464_207246.33333333333334426.0DomainMH1
HgeneSMAD7chr18:46468851chr18:46690157ENST00000262158-3464_207247.33333333333334427.0DomainMH1
HgeneSMAD7chr18:46468851chr18:46690157ENST00000589634-3464_207246.33333333333334426.0DomainMH1
HgeneSMAD7chr18:46468851chr18:46570574ENST00000262158-34208_211247.33333333333334427.0MotifNote=PY-motif
HgeneSMAD7chr18:46468851chr18:46570574ENST00000589634-34208_211246.33333333333334426.0MotifNote=PY-motif
HgeneSMAD7chr18:46468851chr18:46690157ENST00000262158-34208_211247.33333333333334427.0MotifNote=PY-motif
HgeneSMAD7chr18:46468851chr18:46690157ENST00000589634-34208_211246.33333333333334426.0MotifNote=PY-motif

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSMAD7chr18:46468851chr18:46570574ENST00000591805-34207_21032.333333333333336212.0Compositional biasNote=Poly-Pro
HgeneSMAD7chr18:46468851chr18:46570574ENST00000591805-3449_5632.333333333333336212.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46690157ENST00000591805-34207_21032.333333333333336212.0Compositional biasNote=Poly-Pro
HgeneSMAD7chr18:46468851chr18:46690157ENST00000591805-3449_5632.333333333333336212.0Compositional biasNote=Poly-Gly
HgeneSMAD7chr18:46468851chr18:46570574ENST00000262158-34261_426247.33333333333334427.0DomainMH2
HgeneSMAD7chr18:46468851chr18:46570574ENST00000589634-34261_426246.33333333333334426.0DomainMH2
HgeneSMAD7chr18:46468851chr18:46570574ENST00000591805-34261_42632.333333333333336212.0DomainMH2
HgeneSMAD7chr18:46468851chr18:46570574ENST00000591805-3464_20732.333333333333336212.0DomainMH1
HgeneSMAD7chr18:46468851chr18:46690157ENST00000262158-34261_426247.33333333333334427.0DomainMH2
HgeneSMAD7chr18:46468851chr18:46690157ENST00000589634-34261_426246.33333333333334426.0DomainMH2
HgeneSMAD7chr18:46468851chr18:46690157ENST00000591805-34261_42632.333333333333336212.0DomainMH2
HgeneSMAD7chr18:46468851chr18:46690157ENST00000591805-3464_20732.333333333333336212.0DomainMH1
HgeneSMAD7chr18:46468851chr18:46570574ENST00000591805-34208_21132.333333333333336212.0MotifNote=PY-motif
HgeneSMAD7chr18:46468851chr18:46690157ENST00000591805-34208_21132.333333333333336212.0MotifNote=PY-motif


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>68_SMAD7_46468851_DYM_46570574_ranked_0.pdbSMAD74646885146468851ENST00000269445DYMchr1846570574-
MESPPPPYSRYPMDFLKPTADCPDAVPSSAETGGTNYLAPGGLSEISRIEIQICGRGAARGVFYPLCLVSCLQLSSRPVLESTGHPAVHH
130


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
SMAD7_pLDDT.png
all structure
all structure
DYM_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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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
SMAD7
DYM


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 SMAD7-DYM


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 SMAD7-DYM


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