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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:SMO-STRIP2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SMO-STRIP2
FusionPDB ID: 84232
FusionGDB2.0 ID: 84232
HgeneTgene
Gene symbol

SMO

STRIP2

Gene ID

54498

57464

Gene namespermine oxidasestriatin interacting protein 2
SynonymsC20orf16|PAO|PAO-1|PAO1|PAOH|PAOH1|SMOFAM40B|FAR11B
Cytomap

20p13

7q32.1

Type of geneprotein-codingprotein-coding
Descriptionspermine oxidaseflavin containing amine oxidaseflavin-containing spermine oxidasepolyamine oxidase 1putative cyclin G1 interacting proteinstriatin-interacting protein 2FAR11 factor arrest 11 homolog Bfamily with sequence similarity 40, member Bhomolog of yeast FAR11 protein 2protein FAM40B
Modification date2020031320200313
UniProtAcc

SMO

Q9ULQ0

Ensembl transtripts involved in fusion geneENST idsENST00000249373, ENST00000249344, 
ENST00000435494, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 3=1084 X 5 X 5=100
# samples 65
** MAII scorelog2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SMO [Title/Abstract] AND STRIP2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SMO(128849238)-STRIP2(129104453), # samples:1
Anticipated loss of major functional domain due to fusion event.SMO-STRIP2 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.
SMO-STRIP2 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.
SMO-STRIP2 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.
SMO-STRIP2 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.
* 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
HgeneSMO

GO:0006598

polyamine catabolic process

12477380


check buttonFusion gene breakpoints across SMO (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 STRIP2 (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
ChimerDB4HNSCTCGA-DQ-7592-01ASMOchr7

128849238

+STRIP2chr7

129104453

+


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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)
ENST00000249373SMOchr7128849238+ENST00000249344STRIP2chr7129104453+517217462652601778
ENST00000249373SMOchr7128849238+ENST00000435494STRIP2chr7129104453+293617462652373702

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
ENST00000249373ENST00000249344SMOchr7128849238+STRIP2chr7129104453+0.0012204390.9987796
ENST00000249373ENST00000435494SMOchr7128849238+STRIP2chr7129104453+0.0047395550.9952604

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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

>84232_84232_1_SMO-STRIP2_SMO_chr7_128849238_ENST00000249373_STRIP2_chr7_129104453_ENST00000249344_length(amino acids)=778AA_BP=1
MAGLAMAAARPARGPELPLLGLLLLLLLGDPGRGAASSGNATGPGPRSAGGSARRSAAVTGPPPPLSHCGRAAPCEPLRYNVCLGSVLPY
GATSTLLAGDSDSQEEAHGKLVLWSGLRNAPRCWAVIQPLLCAVYMPKCENDRVELPSRTLCQATRGPCAIVERERGWPDFLRCTPDRFP
EGCTNEVQNIKFNSSGQCEVPLVRTDNPKSWYEDVEGCGIQCQNPLFTEAEHQDMHSYIAAFGAVTGLCTLFTLATFVADWRNSNRYPAV
ILFYVNACFFVGSIGWLAQFMDGARREIVCRADGTMRLGEPTSNETLSCVIIFVIVYYALMAGVVWFVVLTYAWHTSFKALGTTYQPLSG
KTSYFHLLTWSLPFVLTVAILAVAQVDGDSVSGICFVGYKNYRYRAGFVLAPIGLVLIVGGYFLIRGVMTLFSIKSNHPGLLSEKAASKI
NETMLRLGIFGFLAFGFVLITFSCHFYDFFNQAEWERSFRDYVLITVLQSMKLGIDVNRHKEIIVKSISTLLLLLLKHFKLNHIYQFEYV
SQHLVFANCIPLILKFFNQNILSYITAKNSISVLDYPCCTIQDLPELTTESLEAGDNSQFCWRNLFSCINLLRLLNKLTKWKHSRTMMLV
VFKSAPILKRALKVKQAMLQLYVLKLLKLQTKYLGRQWRKSNMKTMSAIYQKVRHRMNDDWAYGNDIDARPWDFQAEECTLRANIEAFNS

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

>84232_84232_2_SMO-STRIP2_SMO_chr7_128849238_ENST00000249373_STRIP2_chr7_129104453_ENST00000435494_length(amino acids)=702AA_BP=1
MAGLAMAAARPARGPELPLLGLLLLLLLGDPGRGAASSGNATGPGPRSAGGSARRSAAVTGPPPPLSHCGRAAPCEPLRYNVCLGSVLPY
GATSTLLAGDSDSQEEAHGKLVLWSGLRNAPRCWAVIQPLLCAVYMPKCENDRVELPSRTLCQATRGPCAIVERERGWPDFLRCTPDRFP
EGCTNEVQNIKFNSSGQCEVPLVRTDNPKSWYEDVEGCGIQCQNPLFTEAEHQDMHSYIAAFGAVTGLCTLFTLATFVADWRNSNRYPAV
ILFYVNACFFVGSIGWLAQFMDGARREIVCRADGTMRLGEPTSNETLSCVIIFVIVYYALMAGVVWFVVLTYAWHTSFKALGTTYQPLSG
KTSYFHLLTWSLPFVLTVAILAVAQVDGDSVSGICFVGYKNYRYRAGFVLAPIGLVLIVGGYFLIRGVMTLFSIKSNHPGLLSEKAASKI
NETMLRLGIFGFLAFGFVLITFSCHFYDFFNQAEWERSFRDYVLITVLQSMKLGIDVNRHKEIIVKSISTLLLLLLKHFKLNHIYQFEYV
SQHLVFANCIPLILKFFNQNILSYITAKNSISVLDYPCCTIQDLPELTTESLEAGDNSQFCWRNLFSCINLLRLLNKLTKWKHSRTMMLV

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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/chr7:128849238/chr7:129104453)
- 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
SMO

SMO

STRIP2

Q9ULQ0

555FUNCTION: Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the control of cell shape. {ECO:0000269|PubMed:21834987}.

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
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+81265_181488.6666666666667788.0DomainFZ
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812255_262488.6666666666667788.0Topological domainCytoplasmic
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812284_314488.6666666666667788.0Topological domainExtracellular
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+81228_233488.6666666666667788.0Topological domainExtracellular
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812336_358488.6666666666667788.0Topological domainCytoplasmic
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812380_402488.6666666666667788.0Topological domainExtracellular
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812424_451488.6666666666667788.0Topological domainCytoplasmic
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812234_254488.6666666666667788.0TransmembraneHelical%3B Name%3D1
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812263_283488.6666666666667788.0TransmembraneHelical%3B Name%3D2
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812315_335488.6666666666667788.0TransmembraneHelical%3B Name%3D3
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812359_379488.6666666666667788.0TransmembraneHelical%3B Name%3D4
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812403_423488.6666666666667788.0TransmembraneHelical%3B Name%3D5
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812452_472488.6666666666667788.0TransmembraneHelical%3B Name%3D6
TgeneSTRIP2chr7:128849238chr7:129104453ENST000002493441421577_582549.6666666666666835.0Compositional biasNote=Poly-Leu
TgeneSTRIP2chr7:128849238chr7:129104453ENST000004354941420577_582549.6666666666666759.0Compositional biasNote=Poly-Leu

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812473_524488.6666666666667788.0Topological domainExtracellular
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812546_787488.6666666666667788.0Topological domainCytoplasmic
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812525_545488.6666666666667788.0TransmembraneHelical%3B Name%3D7


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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
SMO
STRIP2


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
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812538_569488.6666666666667788.0BBS5 and BBS7
HgeneSMOchr7:128849238chr7:129104453ENST00000249373+812581_593488.6666666666667788.0DLG5


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Related Drugs to SMO-STRIP2


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 SMO-STRIP2


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