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Fusion gene ID: 22704 |
FusionGeneSummary for MTA2_PTMA |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: MTA2_PTMA | Fusion gene ID: 22704 | Hgene | Tgene | Gene symbol | MTA2 | PTMA | Gene ID | 9219 | 5757 |
| Gene name | metastasis associated 1 family member 2 | prothymosin alpha | |
| Synonyms | MTA1L1|PID | TMSA | |
| Cytomap | 11q12.3 | 2q37.1 | |
| Type of gene | protein-coding | protein-coding | |
| Description | metastasis-associated protein MTA2MTA1-L1 proteinmetastasis -associated gene 1-like 1metastasis associated gene family, member 2metastasis-associated 1-like 1metastasis-associated protein 2p53 target protein in deacetylase complex | prothymosin alphagene sequence 28prothymosin alpha proteinprothymosin-I+/- | |
| Modification date | 20180523 | 20180522 | |
| UniProtAcc | O94776 | P06454 | |
| Ensembl transtripts involved in fusion gene | ENST00000278823, ENST00000524902, ENST00000527204, | ENST00000466801, ENST00000409321, ENST00000409115, ENST00000341369, ENST00000409683, ENST00000410064, | |
| Fusion gene scores | * DoF score | 6 X 6 X 4=144 | 17 X 17 X 2=578 |
| # samples | 6 | 18 | |
| ** MAII score | log2(6/144*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(18/578*10)=-1.683072586171 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: MTA2 [Title/Abstract] AND PTMA [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) |
| 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 information from three resources (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 | BF541543 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| * LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
| 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 |
| intron-3UTR | ENST00000278823 | ENST00000466801 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000278823 | ENST00000409321 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000278823 | ENST00000409115 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000278823 | ENST00000341369 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000278823 | ENST00000409683 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000278823 | ENST00000410064 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000524902 | ENST00000466801 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000524902 | ENST00000409321 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000524902 | ENST00000409115 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000524902 | ENST00000341369 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000524902 | ENST00000409683 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000524902 | ENST00000410064 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000527204 | ENST00000466801 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000527204 | ENST00000409321 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000527204 | ENST00000409115 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000527204 | ENST00000341369 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000527204 | ENST00000409683 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
| intron-3UTR | ENST00000527204 | ENST00000410064 | MTA2 | chr11 | 62361236 | - | PTMA | chr2 | 232576100 | + |
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FusionProtFeatures for MTA2_PTMA |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| MTA2 | PTMA |
| May be involved in the regulation of gene expression asrepressor and activator. The repression might be related tocovalent modification of histone proteins. | Prothymosin alpha may mediate immune function byconferring resistance to certain opportunistic infections. |
| 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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FusionGeneSequence for MTA2_PTMA |
| For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. (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 MTA2_PTMA |
| 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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RelatedDrugs for MTA2_PTMA |
| Drugs targeting genes involved in this fusion gene. (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 MTA2_PTMA |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | MTA2 | C0014175 | Endometriosis | 1 | CTD_human |
| Tgene | PTMA | C0001430 | Adenoma | 1 | CTD_human |
| Tgene | PTMA | C0015695 | Fatty Liver | 1 | CTD_human |
| Tgene | PTMA | C0024121 | Lung Neoplasms | 1 | CTD_human |
| Tgene | PTMA | C0035412 | Rhabdomyosarcoma | 1 | CTD_human |
Copyright 2018-Present -The University of Texas Health Science Center at Houston (UTHealth)
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