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Fusion gene ID: 34957 |
FusionGeneSummary for SMO_TSPAN33 |
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Fusion gene information | Fusion gene name: SMO_TSPAN33 | Fusion gene ID: 34957 | Hgene | Tgene | Gene symbol | SMO | TSPAN33 | Gene ID | 54498 | 340348 |
Gene name | spermine oxidase | tetraspanin 33 | |
Synonyms | C20orf16|PAO|PAO-1|PAO1|PAOH|PAOH1|SMO | PEN|PEN.|TSPAN-33 | |
Cytomap | 20p13 | 7q32.1 | |
Type of gene | protein-coding | protein-coding | |
Description | spermine oxidaseflavin containing amine oxidaseflavin-containing spermine oxidasepolyamine oxidase 1putative cyclin G1 interacting protein | tetraspanin-33penumbraproerythroblast new membrane | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | Q99835 | Q86UF1 | |
Ensembl transtripts involved in fusion gene | ENST00000249373, | ENST00000289407, | |
Fusion gene scores | * DoF score | 6 X 6 X 3=108 | 3 X 1 X 3=9 |
# samples | 7 | 3 | |
** MAII score | log2(7/108*10)=-0.625604485218502 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(3/9*10)=1.73696559416621 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: SMO [Title/Abstract] AND TSPAN33 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | SMO | GO:0006598 | polyamine catabolic process | 12477380 |
Tgene | TSPAN33 | GO:0051604 | protein maturation | 23091066 |
Tgene | TSPAN33 | GO:0072659 | protein localization to plasma membrane | 23091066 |
![]() (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * 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. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | RV | LUSC | TCGA-NC-A5HT-01A | SMO | chr7 | 128829323 | + | TSPAN33 | chr7 | 128801520 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
Frame-shift | ENST00000249373 | ENST00000289407 | SMO | chr7 | 128829323 | + | TSPAN33 | chr7 | 128801520 | + |
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FusionProtFeatures for SMO_TSPAN33 |
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Hgene | Tgene |
SMO | TSPAN33 |
G protein-coupled receptor that probably associates withthe patched protein (PTCH) to transduce the hedgehog's proteinssignal. Binding of sonic hedgehog (SHH) to its receptor patched isthought to prevent normal inhibition by patched of smoothened(SMO). Required for the accumulation of KIF7, GLI2 and GLI3 in thecilia (PubMed:19592253). Interacts with DLG5 at the ciliary baseto induce the accumulation of KIF7 and GLI2 at the ciliary tip forGLI2 activation (By similarity). {ECO:0000250|UniProtKB:P56726,ECO:0000269|PubMed:19592253}. | Plays an important role in normal erythropoiesis (Bysimilarity). It has a role in the differentiation of erythroidprogenitors (By similarity). Regulates maturation and traffickingof the transmembrane metalloprotease ADAM10 (PubMed:26686862).Negatively regulates ligand-induced Notch activity probably byregulating ADAM10 activity (PubMed:26686862).{ECO:0000250|UniProtKB:Q8R3S2, ECO:0000269|PubMed:26686862}. |
![]() * Minus value of BPloci means that the break pointn is located before the CDS. |
- In-frame and retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for SMO_TSPAN33 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for SMO_TSPAN33 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
SMO | PTCH1, PTCH2, BCL6, NEDD4, CHEK1, ATM, KIT, FAM189B | TSPAN33 | ADAM10, MSN, PDZD11, PLEKHA7, EZR, LMNA |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for SMO_TSPAN33 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | SMO | Q99835 | DB01047 | Fluocinonide | Smoothened homolog | small molecule | approved|investigational |
Hgene | SMO | Q99835 | DB08828 | Vismodegib | Smoothened homolog | small molecule | approved|investigational |
Hgene | SMO | Q99835 | DB09143 | Sonidegib | Smoothened homolog | small molecule | approved|investigational |
Hgene | SMO | Q99835 | DB06786 | Halcinonide | Smoothened homolog | small molecule | approved|investigational|withdrawn |
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RelatedDiseases for SMO_TSPAN33 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | SMO | C0007117 | Basal cell carcinoma | 2 | CTD_human;HPO |
Hgene | SMO | C0002448 | Ameloblastoma | 1 | CTD_human |
Hgene | SMO | C0006118 | Brain Neoplasms | 1 | CTD_human |
Hgene | SMO | C0022360 | Jaw Abnormalities | 1 | CTD_human |
Hgene | SMO | C0023487 | Acute Promyelocytic Leukemia | 1 | CTD_human |
Hgene | SMO | C0024954 | Maxillary Neoplasms | 1 | CTD_human |
Hgene | SMO | C0025286 | Meningioma | 1 | CTD_human |
Hgene | SMO | C0037286 | Skin Neoplasms | 1 | CTD_human |
Hgene | SMO | C0206663 | Neuroectodermal Tumor, Primitive | 1 | CTD_human |
Hgene | SMO | C0795915 | Winter Shortland Temple syndrome | 1 | ORPHANET;UNIPROT |