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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:SMU1-AQP3

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SMU1-AQP3
FusionPDB ID: 84291
FusionGDB2.0 ID: 84291
HgeneTgene
Gene symbol

SMU1

AQP3

Gene ID

55234

360

Gene nameSMU1 DNA replication regulator and spliceosomal factoraquaporin 3 (Gill blood group)
SynonymsBWD|SMU-1|fSAP57AQP-3|GIL
Cytomap

9p21.1

9p13.3

Type of geneprotein-codingprotein-coding
DescriptionWD40 repeat-containing protein SMU1DNA replication regulator and spliceosomal factorbrain-enriched WD-repeat proteinfunctional spliceosome-associated protein 57smu-1 suppressor of mec-8 and unc-52 homologsmu-1 suppressor of mec-8 and unc-52 protein haquaporin-3aquaglyceroporin-3aquaporin 3 (GIL blood group)
Modification date2020031320200329
UniProtAcc.

Q92482

Ensembl transtripts involved in fusion geneENST idsENST00000397149, ENST00000536631, 
ENST00000493581, ENST00000297991, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 7 X 7=4413 X 2 X 3=18
# samples 93
** MAII scorelog2(9/441*10)=-2.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SMU1 [Title/Abstract] AND AQP3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SMU1(33068822)-AQP3(33443890), # samples:1
Anticipated loss of major functional domain due to fusion event.SMU1-AQP3 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.
SMU1-AQP3 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.
SMU1-AQP3 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.
SMU1-AQP3 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.
SMU1-AQP3 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SMU1-AQP3 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneSMU1

GO:0000398

mRNA splicing, via spliceosome

28781166

TgeneAQP3

GO:0002684

positive regulation of immune system process

17943189

TgeneAQP3

GO:0006833

water transport

30420639

TgeneAQP3

GO:0015793

glycerol transport

30420639

TgeneAQP3

GO:0032526

response to retinoic acid

17943189

TgeneAQP3

GO:0071456

cellular response to hypoxia

24462679


check buttonFusion gene breakpoints across SMU1 (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 AQP3 (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
ChimerDB4STADTCGA-CD-A4MH-01ASMU1chr9

33068822

-AQP3chr9

33443890

-


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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)
ENST00000397149SMU1chr933068822-ENST00000297991AQP3chr933443890-2212552511322423

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
ENST00000397149ENST00000297991SMU1chr933068822-AQP3chr933443890-0.000504920.999495

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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

>84291_84291_1_SMU1-AQP3_SMU1_chr9_33068822_ENST00000397149_AQP3_chr9_33443890_ENST00000297991_length(amino acids)=423AA_BP=166
MSIEIESSDVIRLIMQYLKENSLHRALATLQEETTVSLNTVDSIESFVADINSGHWDTVLQAIQSLKLPDKTLIDLYEQVVLELIELREL
GAARSLLRQTDPMIMLKQTQPERYIHLENLLARSYFDPREAYPDGSSKEKRRAAIAQALAGEVSVVPPSRLMALLGQMFGCGSVAQVVLS
RGTHGGFLTINLAFGFAVTLGILIAGQVSGAHLNPAVTFAMCFLAREPWIKLPIYTLAQTLGAFLGAGIVFGLYYDAIWHFADNQLFVSG
PNGTAGIFATYPSGHLDMINGFFDQFIGTASLIVCVLAIVDPYNNPVPRGLEAFTVGLVVLVIGTSMGFNSGYAVNPARDFGPRLFTALA

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

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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/chr9:33068822/chr9:33443890)
- 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
.AQP3

Q92482

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: Water channel required to promote glycerol permeability and water transport across cell membranes (PubMed:12239222, PubMed:30420639). Acts as a glycerol transporter in skin and plays an important role in regulating SC (stratum corneum) and epidermal glycerol content. Involved in skin hydration, wound healing, and tumorigenesis. Provides kidney medullary collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient. Slightly permeable to urea and may function as a water and urea exit mechanism in antidiuresis in collecting duct cells. It may play an important role in gastrointestinal tract water transport and in glycerol metabolism (By similarity). {ECO:0000250|UniProtKB:Q8R2N1, ECO:0000269|PubMed:12239222, ECO:0000269|PubMed:30420639}.

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
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-41240_92167.0514.0DomainCTLH
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-4126_38167.0514.0DomainLisH
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106209_22736.0293.0IntramembraneDiscontinuously helical
TgeneAQP3chr9:33068822chr9:33443890ENST000002979910679_9236.0293.0IntramembraneDiscontinuously helical
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106215_21736.0293.0MotifNPA 2
TgeneAQP3chr9:33068822chr9:33443890ENST000002979910683_8536.0293.0MotifNPA 1
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106124_15736.0293.0Topological domainExtracellular
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106179_18836.0293.0Topological domainCytoplasmic
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106228_24436.0293.0Topological domainExtracellular
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106266_29236.0293.0Topological domainCytoplasmic
TgeneAQP3chr9:33068822chr9:33443890ENST000002979910648_5336.0293.0Topological domainExtracellular
TgeneAQP3chr9:33068822chr9:33443890ENST000002979910675_7836.0293.0Topological domainCytoplasmic
TgeneAQP3chr9:33068822chr9:33443890ENST000002979910693_9836.0293.0Topological domainCytoplasmic
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106158_17836.0293.0TransmembraneHelical
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106189_20836.0293.0TransmembraneHelical
TgeneAQP3chr9:33068822chr9:33443890ENST0000029799106245_26536.0293.0TransmembraneHelical
TgeneAQP3chr9:33068822chr9:33443890ENST000002979910654_7436.0293.0TransmembraneHelical
TgeneAQP3chr9:33068822chr9:33443890ENST000002979910699_12336.0293.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-412212_253167.0514.0RepeatWD 1
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-412262_303167.0514.0RepeatWD 2
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-412305_346167.0514.0RepeatWD 3
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-412347_386167.0514.0RepeatWD 4
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-412395_436167.0514.0RepeatWD 5
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-412440_479167.0514.0RepeatWD 6
HgeneSMU1chr9:33068822chr9:33443890ENST00000397149-412482_513167.0514.0RepeatWD 7
TgeneAQP3chr9:33068822chr9:33443890ENST00000297991061_2636.0293.0Topological domainCytoplasmic
TgeneAQP3chr9:33068822chr9:33443890ENST000002979910627_4736.0293.0TransmembraneHelical


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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
SMU1
AQP3


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 SMU1-AQP3


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 SMU1-AQP3


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