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Fusion Protein:SPG7-MOB1A |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: SPG7-MOB1A | FusionPDB ID: 85761 | FusionGDB2.0 ID: 85761 | Hgene | Tgene | Gene symbol | SPG7 | MOB1A | Gene ID | 6687 | 55233 |
| Gene name | SPG7 matrix AAA peptidase subunit, paraplegin | MOB kinase activator 1A | |
| Synonyms | CAR|CMAR|PGN|SPG5C | C2orf6|MATS1|MOB1|MOBK1B|MOBKL1B|Mob4B | |
| Cytomap | 16q24.3 | 2p13.1 | |
| Type of gene | protein-coding | protein-coding | |
| Description | parapleginSPG7, paraplegin matrix AAA peptidase subunitcell matrix adhesion regulatorspastic paraplegia 7 (pure and complicated autosomal recessive)spastic paraplegia 7 protein | MOB kinase activator 1AMOB1 Mps One Binder homolog AMOB1, Mps One Binder kinase activator-like 1Bmob1 alphamob1 homolog 1Bmps one binder kinase activator-like 1B | |
| Modification date | 20200320 | 20200313 | |
| UniProtAcc | . | Q9H8S9 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000268704, ENST00000341316, ENST00000565891, | ENST00000409969, ENST00000497054, ENST00000396049, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 10 X 7 X 6=420 | 6 X 6 X 4=144 |
| # samples | 10 | 6 | |
| ** MAII score | log2(10/420*10)=-2.0703893278914 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(6/144*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: SPG7 [Title/Abstract] AND MOB1A [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | SPG7(89579445)-MOB1A(74394234), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | SPG7-MOB1A seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. SPG7-MOB1A seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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 |
| Tgene | MOB1A | GO:0035329 | hippo signaling | 19739119 |
| Fusion gene breakpoints across SPG7 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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| Fusion gene breakpoints across MOB1A (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
| Fusion gene information from FusionGDB2.0. |
| 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-HU-A4GN-01A | SPG7 | chr16 | 89579445 | + | MOB1A | chr2 | 74394234 | - |
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Fusion ORF Analysis |
| Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
| 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) |
| ENST00000268704 | SPG7 | chr16 | 89579445 | + | ENST00000396049 | MOB1A | chr2 | 74394234 | - | 4901 | 391 | 15 | 860 | 281 |
| ENST00000341316 | SPG7 | chr16 | 89579445 | + | ENST00000396049 | MOB1A | chr2 | 74394234 | - | 4893 | 383 | 7 | 852 | 281 |
| 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 |
| ENST00000268704 | ENST00000396049 | SPG7 | chr16 | 89579445 | + | MOB1A | chr2 | 74394234 | - | 0.000354864 | 0.9996451 |
| ENST00000341316 | ENST00000396049 | SPG7 | chr16 | 89579445 | + | MOB1A | chr2 | 74394234 | - | 0.000352178 | 0.99964786 |
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Fusion Amino Acid Sequences |
| For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
| >FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >85761_85761_1_SPG7-MOB1A_SPG7_chr16_89579445_ENST00000268704_MOB1A_chr2_74394234_ENST00000396049_length(amino acids)=281AA_BP=125 MAVLLLLLRALRRGPGPGPRPLWGPGPAWSPGFPARPGRGRPYMASRPPGDLAEAGGRALQSLQLRLLTPTFEGINGLLLKQHLVQNPVR LWQLLGGTFYFNTSRLKQKNKEKDKSKGKAPEEDEAVDFFNQINMLYGTITEFCTEASCPVMSAGPRYEYHWADGTNIKKPIKCSAPKYI DYLMTWVQDQLDDETLFPSKIGVPFPKNFMSVAKTILKRLFRVYAHIYHQHFDSVMQLQEEAHLNTSFKHFIFFVQEFNLIDRRELAPLQ -------------------------------------------------------------- >85761_85761_2_SPG7-MOB1A_SPG7_chr16_89579445_ENST00000341316_MOB1A_chr2_74394234_ENST00000396049_length(amino acids)=281AA_BP=125 MAVLLLLLRALRRGPGPGPRPLWGPGPAWSPGFPARPGRGRPYMASRPPGDLAEAGGRALQSLQLRLLTPTFEGINGLLLKQHLVQNPVR LWQLLGGTFYFNTSRLKQKNKEKDKSKGKAPEEDEAVDFFNQINMLYGTITEFCTEASCPVMSAGPRYEYHWADGTNIKKPIKCSAPKYI DYLMTWVQDQLDDETLFPSKIGVPFPKNFMSVAKTILKRLFRVYAHIYHQHFDSVMQLQEEAHLNTSFKHFIFFVQEFNLIDRRELAPLQ -------------------------------------------------------------- |
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Fusion Protein Functional Features |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr16:89579445/chr2:74394234) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| . | MOB1A |
| FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. | FUNCTION: Activator of LATS1/2 in the Hippo signaling pathway which plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis. The core of this pathway is composed of a kinase cascade wherein STK3/MST2 and STK4/MST1, in complex with its regulatory protein SAV1, phosphorylates and activates LATS1/2 in complex with its regulatory protein MOB1, which in turn phosphorylates and inactivates YAP1 oncoprotein and WWTR1/TAZ. Phosphorylation of YAP1 by LATS1/2 inhibits its translocation into the nucleus to regulate cellular genes important for cell proliferation, cell death, and cell migration. Stimulates the kinase activity of STK38 and STK38L. Acts cooperatively with STK3/MST2 to activate STK38. {ECO:0000269|PubMed:15197186, ECO:0000269|PubMed:18362890, 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. |
| - 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 |
| - 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 |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000268704 | + | 3 | 17 | 349_357 | 125.33333333333333 | 796.0 | Nucleotide binding | ATP |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000341316 | + | 3 | 10 | 349_357 | 125.33333333333333 | 490.0 | Nucleotide binding | ATP |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000268704 | + | 3 | 17 | 106_144 | 125.33333333333333 | 796.0 | Topological domain | Mitochondrial matrix |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000268704 | + | 3 | 17 | 166_248 | 125.33333333333333 | 796.0 | Topological domain | Mitochondrial intermembrane |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000268704 | + | 3 | 17 | 270_795 | 125.33333333333333 | 796.0 | Topological domain | Mitochondrial matrix |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000341316 | + | 3 | 10 | 106_144 | 125.33333333333333 | 490.0 | Topological domain | Mitochondrial matrix |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000341316 | + | 3 | 10 | 166_248 | 125.33333333333333 | 490.0 | Topological domain | Mitochondrial intermembrane |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000341316 | + | 3 | 10 | 270_795 | 125.33333333333333 | 490.0 | Topological domain | Mitochondrial matrix |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000268704 | + | 3 | 17 | 145_165 | 125.33333333333333 | 796.0 | Transmembrane | Helical |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000268704 | + | 3 | 17 | 249_269 | 125.33333333333333 | 796.0 | Transmembrane | Helical |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000341316 | + | 3 | 10 | 145_165 | 125.33333333333333 | 490.0 | Transmembrane | Helical |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000341316 | + | 3 | 10 | 249_269 | 125.33333333333333 | 490.0 | Transmembrane | Helical |
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Fusion Protein-Protein Interaction |
| 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 from validated records (BIOGRID-3.4.160) |
| Gene | PPI interactors |
| Protein-protein interactors based on sequence similarity (STRING) |
| Gene | STRING network |
| SPG7 | |
| MOB1A |
| - Retained interactions in fusion protein (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost interactions due to fusion (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000268704 | + | 3 | 17 | 701_795 | 125.33333333333333 | 796.0 | PPIF |
| Hgene | SPG7 | chr16:89579445 | chr2:74394234 | ENST00000341316 | + | 3 | 10 | 701_795 | 125.33333333333333 | 490.0 | PPIF |
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Related Drugs to SPG7-MOB1A |
| Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to SPG7-MOB1A |
| Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Disease | Source | PMID |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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