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Fusion gene ID: 535 |
FusionGeneSummary for ACTB_THBS3 |
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Fusion gene information | Fusion gene name: ACTB_THBS3 | Fusion gene ID: 535 | Hgene | Tgene | Gene symbol | ACTB | THBS3 | Gene ID | 60 | 7059 |
Gene name | actin beta | thrombospondin 3 | |
Synonyms | BRWS1|PS1TP5BP1 | TSP3 | |
Cytomap | 7p22.1 | 1q22 | |
Type of gene | protein-coding | protein-coding | |
Description | actin, cytoplasmic 1I(2)-actinPS1TP5-binding protein 1beta cytoskeletal actin | thrombospondin-3 | |
Modification date | 20180522 | 20180519 | |
UniProtAcc | P60709 | P49746 | |
Ensembl transtripts involved in fusion gene | ENST00000464611, ENST00000331789, | ENST00000368378, ENST00000541576, ENST00000457183, ENST00000541990, ENST00000486260, | |
Fusion gene scores | * DoF score | 28 X 19 X 14=7448 | 6 X 6 X 2=72 |
# samples | 37 | 7 | |
** MAII score | log2(37/7448*10)=-4.33125589704248 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(7/72*10)=-0.0406419844973459 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ACTB [Title/Abstract] AND THBS3 [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 | ACTB | GO:0098974 | postsynaptic actin cytoskeleton organization | 18341992 |
![]() (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 |
ChiTaRS3.1 | BP286903 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
* 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 |
intron-intron | ENST00000464611 | ENST00000368378 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-intron | ENST00000464611 | ENST00000541576 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-intron | ENST00000464611 | ENST00000457183 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-intron | ENST00000464611 | ENST00000541990 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-5UTR | ENST00000464611 | ENST00000486260 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-intron | ENST00000331789 | ENST00000368378 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-intron | ENST00000331789 | ENST00000541576 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-intron | ENST00000331789 | ENST00000457183 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-intron | ENST00000331789 | ENST00000541990 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
intron-5UTR | ENST00000331789 | ENST00000486260 | ACTB | chr7 | 5568898 | - | THBS3 | chr1 | 155178773 | - |
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FusionProtFeatures for ACTB_THBS3 |
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Hgene | Tgene |
ACTB | THBS3 |
Adhesive glycoprotein that mediates cell-to-cell andcell-to-matrix interactions. Can bind to fibrinogen, fibronectin,laminin and type V collagen. |
![]() * 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 ACTB_THBS3 |
![]() (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 ACTB_THBS3 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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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 ACTB_THBS3 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for ACTB_THBS3 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ACTB | C2239176 | Liver carcinoma | 2 | CTD_human |
Hgene | ACTB | C0005586 | Bipolar Disorder | 1 | PSYGENET |
Hgene | ACTB | C0009363 | Congenital ocular coloboma (disorder) | 1 | CTD_human |
Hgene | ACTB | C0013393 | Dysostoses | 1 | CTD_human |
Hgene | ACTB | C0013421 | Dystonia | 1 | CTD_human |
Hgene | ACTB | C0014859 | Esophageal Neoplasms | 1 | CTD_human |
Hgene | ACTB | C0018784 | Sensorineural Hearing Loss (disorder) | 1 | CTD_human;HPO |
Hgene | ACTB | C0024121 | Lung Neoplasms | 1 | CTD_human |
Hgene | ACTB | C0024667 | Animal Mammary Neoplasms | 1 | CTD_human |
Hgene | ACTB | C0024668 | Mammary Neoplasms, Experimental | 1 | CTD_human |
Hgene | ACTB | C0027626 | Neoplasm Invasiveness | 1 | CTD_human |
Hgene | ACTB | C0029408 | Degenerative polyarthritis | 1 | CTD_human |
Hgene | ACTB | C0036341 | Schizophrenia | 1 | PSYGENET |
Hgene | ACTB | C0151744 | Myocardial Ischemia | 1 | CTD_human |
Hgene | ACTB | C0242184 | Hypoxia | 1 | CTD_human |
Hgene | ACTB | C0376634 | Craniofacial Abnormalities | 1 | CTD_human |
Hgene | ACTB | C0497552 | Congenital neurologic anomalies | 1 | CTD_human |
Hgene | ACTB | C1846331 | Juvenile-onset dystonia | 1 | CTD_human;ORPHANET;UNIPROT |
Hgene | ACTB | C1855722 | Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation | 1 | ORPHANET;UNIPROT |