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Fusion Gene Summary | |
Fusion Gene ORF analysis | |
Fusion Genomic Features | |
Fusion Protein Features | |
Fusion Gene Sequence | |
Fusion Gene PPI analysis | |
Related Drugs | |
Related Diseases |
Fusion gene:MYO10-CD2AP (FusionGDB2 ID:56203) |
Fusion Gene Summary for MYO10-CD2AP |
Fusion gene summary |
Fusion gene information | Fusion gene name: MYO10-CD2AP | Fusion gene ID: 56203 | Hgene | Tgene | Gene symbol | MYO10 | CD2AP | Gene ID | 4651 | 23607 |
Gene name | myosin X | CD2 associated protein | |
Synonyms | - | CMS | |
Cytomap | 5p15.1 | 6p12.3 | |
Type of gene | protein-coding | protein-coding | |
Description | unconventional myosin-Xunconventional myosin-10unconventionnal myosin-X | CD2-associated proteinCas ligand with multiple Src homology 3 (SH3) domainsadapter protein CMScas ligand with multiple SH3 domains | |
Modification date | 20200313 | 20200327 | |
UniProtAcc | Q9HD67 | Q9Y5K6 | |
Ensembl transtripts involved in fusion gene | ENST00000513610, ENST00000507288, ENST00000274203, ENST00000515803, ENST00000427430, ENST00000505695, ENST00000512061, | ENST00000359314, ENST00000486693, | |
Fusion gene scores | * DoF score | 20 X 14 X 10=2800 | 12 X 12 X 8=1152 |
# samples | 25 | 14 | |
** MAII score | log2(25/2800*10)=-3.48542682717024 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(14/1152*10)=-3.04064198449735 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: MYO10 [Title/Abstract] AND CD2AP [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | MYO10(16935897)-CD2AP(47563597), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | MYO10-CD2AP 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) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Fusion gene breakpoints across MYO10 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
Fusion gene breakpoints across CD2AP (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | STAD | TCGA-BR-8678-01A | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
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Fusion Gene ORF analysis for MYO10-CD2AP |
Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * 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 | ENST00000513610 | ENST00000359314 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
5CDS-intron | ENST00000513610 | ENST00000486693 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
Frame-shift | ENST00000507288 | ENST00000359314 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
5CDS-intron | ENST00000507288 | ENST00000486693 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-3CDS | ENST00000274203 | ENST00000359314 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-intron | ENST00000274203 | ENST00000486693 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-3CDS | ENST00000515803 | ENST00000359314 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-intron | ENST00000515803 | ENST00000486693 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-3CDS | ENST00000427430 | ENST00000359314 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-intron | ENST00000427430 | ENST00000486693 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-3CDS | ENST00000505695 | ENST00000359314 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-intron | ENST00000505695 | ENST00000486693 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-3CDS | ENST00000512061 | ENST00000359314 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
intron-intron | ENST00000512061 | ENST00000486693 | MYO10 | chr5 | 16935897 | - | CD2AP | chr6 | 47563597 | + |
ORFfinder result based on the fusion transcript sequence of in-frame fusion genes. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
DeepORF 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. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for MYO10-CD2AP |
FusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints. |
Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page. |
Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page. |
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Fusion Protein Features for MYO10-CD2AP |
Go to FGviewer for the breakpoints of :-: - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
MYO10 | CD2AP |
FUNCTION: Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. MYO10 binds to actin filaments and actin bundles and functions as plus end-directed motor. The tail domain binds to membranous compartments containing phosphatidylinositol 3,4,5-trisphosphate or integrins, and mediates cargo transport along actin filaments. Regulates cell shape, cell spreading and cell adhesion. Stimulates the formation and elongation of filopodia. May play a role in neurite outgrowth and axon guidance. In hippocampal neurons it induces the formation of dendritic filopodia by trafficking the actin-remodeling protein VASP to the tips of filopodia, where it promotes actin elongation. Plays a role in formation of the podosome belt in osteoclasts. {ECO:0000269|PubMed:16894163, ECO:0000269|PubMed:18570893}.; FUNCTION: [Isoform Headless]: Functions as a dominant-negative regulator of isoform 1, suppressing its filopodia-inducing and axon outgrowth-promoting activities. In hippocampal neurons, it increases VASP retention in spine heads to induce spine formation and spine head expansion (By similarity). {ECO:0000250}. | FUNCTION: Seems to act as an adapter protein between membrane proteins and the actin cytoskeleton (PubMed:10339567). In collaboration with CBLC, modulates the rate of RET turnover and may act as regulatory checkpoint that limits the potency of GDNF on neuronal survival. Controls CBLC function, converting it from an inhibitor to a promoter of RET degradation (By similarity). May play a role in receptor clustering and cytoskeletal polarity in the junction between T-cell and antigen-presenting cell (By similarity). May anchor the podocyte slit diaphragm to the actin cytoskeleton in renal glomerolus. Also required for cytokinesis (PubMed:15800069). Plays a role in epithelial cell junctions formation (PubMed:22891260). {ECO:0000250|UniProtKB:F1LRS8, ECO:0000250|UniProtKB:Q9JLQ0, ECO:0000269|PubMed:10339567, ECO:0000269|PubMed:15800069, ECO:0000269|PubMed:22891260}. |
Retention 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 * 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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Fusion Gene Sequence for MYO10-CD2AP |
For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
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Fusion Gene PPI Analysis for MYO10-CD2AP |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
- Retained PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
- Retained PPIs, but lost function due to frame-shift fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for MYO10-CD2AP |
Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for MYO10-CD2AP |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | MYO10 | C0043094 | Weight Gain | 1 | CTD_human |
Tgene | CD2AP | C0002395 | Alzheimer's Disease | 3 | CTD_human |
Tgene | CD2AP | C0011265 | Presenile dementia | 3 | CTD_human |
Tgene | CD2AP | C0276496 | Familial Alzheimer Disease (FAD) | 3 | CTD_human |
Tgene | CD2AP | C0494463 | Alzheimer Disease, Late Onset | 3 | CTD_human |
Tgene | CD2AP | C0546126 | Acute Confusional Senile Dementia | 3 | CTD_human |
Tgene | CD2AP | C0750900 | Alzheimer's Disease, Focal Onset | 3 | CTD_human |
Tgene | CD2AP | C0750901 | Alzheimer Disease, Early Onset | 3 | CTD_human |
Tgene | CD2AP | C1842982 | FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO | 2 | GENOMICS_ENGLAND |
Tgene | CD2AP | C1868672 | NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE | 1 | ORPHANET |