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Fusion gene ID: 22248 |
FusionGeneSummary for MOB1B_MOB1B |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: MOB1B_MOB1B | Fusion gene ID: 22248 | Hgene | Tgene | Gene symbol | MOB1B | MOB1B | Gene ID | 92597 | 92597 |
| Gene name | MOB kinase activator 1B | MOB kinase activator 1B | |
| Synonyms | MATS2|MOB4A|MOBKL1A | MATS2|MOB4A|MOBKL1A | |
| Cytomap | 4q13.3 | 4q13.3 | |
| Type of gene | protein-coding | protein-coding | |
| Description | MOB kinase activator 1BMOB1 Mps One Binder homolog BMOB1, Mps One Binder kinase activator-like 1Amob1 homolog 1Amob1Amps one binder kinase activator-like 1A | MOB kinase activator 1BMOB1 Mps One Binder homolog BMOB1, Mps One Binder kinase activator-like 1Amob1 homolog 1Amob1Amps one binder kinase activator-like 1A | |
| Modification date | 20180519 | 20180519 | |
| UniProtAcc | Q7L9L4 | Q7L9L4 | |
| Ensembl transtripts involved in fusion gene | ENST00000309395, ENST00000396051, ENST00000511449, | ENST00000309395, ENST00000396051, ENST00000511449, | |
| Fusion gene scores | * DoF score | 4 X 2 X 4=32 | 2 X 2 X 2=8 |
| # samples | 4 | 2 | |
| ** MAII score | log2(4/32*10)=0.321928094887362 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(2/8*10)=1.32192809488736 | |
| Context | PubMed: MOB1B [Title/Abstract] AND MOB1B [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 |
| Hgene | MOB1B | GO:0031952 | regulation of protein autophosphorylation | 15197186 |
| Hgene | MOB1B | GO:0035329 | hippo signaling | 19739119 |
| Tgene | MOB1B | GO:0031952 | regulation of protein autophosphorylation | 15197186 |
| Tgene | MOB1B | GO:0035329 | hippo signaling | 19739119 |
| 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 | CV342709 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| * 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-intron | ENST00000309395 | ENST00000309395 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| intron-intron | ENST00000309395 | ENST00000396051 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| intron-intron | ENST00000309395 | ENST00000511449 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| intron-intron | ENST00000396051 | ENST00000309395 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| intron-intron | ENST00000396051 | ENST00000396051 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| intron-intron | ENST00000396051 | ENST00000511449 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| intron-intron | ENST00000511449 | ENST00000309395 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| intron-intron | ENST00000511449 | ENST00000396051 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
| intron-intron | ENST00000511449 | ENST00000511449 | MOB1B | chr4 | 71795726 | - | MOB1B | chr4 | 71836917 | - |
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FusionProtFeatures for MOB1B_MOB1B |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| MOB1B | MOB1B |
| Activator of LATS1/2 in the Hippo signaling pathwaywhich plays a pivotal role in organ size control and tumorsuppression by restricting proliferation and promoting apoptosis.The core of this pathway is composed of a kinase cascade whereinSTK3/MST2 and STK4/MST1, in complex with its regulatory proteinSAV1, phosphorylates and activates LATS1/2 in complex with itsregulatory protein MOB1, which in turn phosphorylates andinactivates YAP1 oncoprotein and WWTR1/TAZ. Phosphorylation ofYAP1 by LATS1/2 inhibits its translocation into the nucleus toregulate cellular genes important for cell proliferation, celldeath, and cell migration. Stimulates the kinase activity ofSTK38L. {ECO:0000269|PubMed:15067004,ECO:0000269|PubMed:19739119}. | Activator of LATS1/2 in the Hippo signaling pathwaywhich plays a pivotal role in organ size control and tumorsuppression by restricting proliferation and promoting apoptosis.The core of this pathway is composed of a kinase cascade whereinSTK3/MST2 and STK4/MST1, in complex with its regulatory proteinSAV1, phosphorylates and activates LATS1/2 in complex with itsregulatory protein MOB1, which in turn phosphorylates andinactivates YAP1 oncoprotein and WWTR1/TAZ. Phosphorylation ofYAP1 by LATS1/2 inhibits its translocation into the nucleus toregulate cellular genes important for cell proliferation, celldeath, and cell migration. Stimulates the kinase activity ofSTK38L. {ECO:0000269|PubMed:15067004,ECO:0000269|PubMed:19739119}. |
| 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 MOB1B_MOB1B |
| 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 MOB1B_MOB1B |
| 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 MOB1B_MOB1B |
| 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 MOB1B_MOB1B |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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