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Fusion Protein:SPIDR-FNTA |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: SPIDR-FNTA | FusionPDB ID: 85789 | FusionGDB2.0 ID: 85789 | Hgene | Tgene | Gene symbol | SPIDR | FNTA | Gene ID | 23514 | 2339 |
| Gene name | scaffold protein involved in DNA repair | farnesyltransferase, CAAX box, alpha | |
| Synonyms | KIAA0146 | FPTA|PGGT1A|PTAR2 | |
| Cytomap | 8q11.21 | 8p11.21 | |
| Type of gene | protein-coding | protein-coding | |
| Description | DNA repair-scaffolding proteinscaffolding protein involved in DNA repair | protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alphaFTase-alphaGGTase-I-alphafarnesyl-protein transferase alpha-subunitprotein prenyltransferase alpha subunit repeat containing 2ras proteins prenyltransferase subunit alphatype | |
| Modification date | 20200320 | 20200313 | |
| UniProtAcc | Q14159 | P49354 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000521214, ENST00000297423, ENST00000518074, ENST00000541342, ENST00000517693, ENST00000518060, | ENST00000302279, ENST00000342116, ENST00000524546, ENST00000529687, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 24 X 12 X 15=4320 | 10 X 11 X 7=770 |
| # samples | 27 | 14 | |
| ** MAII score | log2(27/4320*10)=-4 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(14/770*10)=-2.4594316186373 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: SPIDR [Title/Abstract] AND FNTA [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | FNTA(42932507)-SPIDR(48192450), # samples:1 SPIDR(48353104)-FNTA(42938261), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | SPIDR-FNTA 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. SPIDR-FNTA 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. FNTA-SPIDR seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. FNTA-SPIDR seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF. FNTA-SPIDR seems lost the major protein functional domain in Tgene 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 |
| Hgene | SPIDR | GO:0006974 | cellular response to DNA damage stimulus | 23509288 |
| Hgene | SPIDR | GO:0010569 | regulation of double-strand break repair via homologous recombination | 23754376 |
| Hgene | SPIDR | GO:0031334 | positive regulation of protein complex assembly | 23509288 |
| Hgene | SPIDR | GO:0070202 | regulation of establishment of protein localization to chromosome | 23509288 |
| Hgene | SPIDR | GO:0071479 | cellular response to ionizing radiation | 23509288|23754376 |
| Hgene | SPIDR | GO:0072711 | cellular response to hydroxyurea | 23509288 |
| Hgene | SPIDR | GO:0072757 | cellular response to camptothecin | 23509288 |
| Tgene | FNTA | GO:0018343 | protein farnesylation | 16893176|19228685 |
| Tgene | FNTA | GO:0018344 | protein geranylgeranylation | 16893176 |
| Tgene | FNTA | GO:0090044 | positive regulation of tubulin deacetylation | 19228685 |
| Tgene | FNTA | GO:0090045 | positive regulation of deacetylase activity | 19228685 |
| Fusion gene breakpoints across SPIDR (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 FNTA (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 | LUAD | TCGA-69-7760-01A | SPIDR | chr8 | 48353104 | + | FNTA | chr8 | 42938261 | + |
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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) |
| ENST00000297423 | SPIDR | chr8 | 48353104 | + | ENST00000302279 | FNTA | chr8 | 42938261 | + | 2345 | 1481 | 51 | 1481 | 476 |
| ENST00000297423 | SPIDR | chr8 | 48353104 | + | ENST00000342116 | FNTA | chr8 | 42938261 | + | 2337 | 1481 | 51 | 1481 | 476 |
| ENST00000518074 | SPIDR | chr8 | 48353104 | + | ENST00000302279 | FNTA | chr8 | 42938261 | + | 1952 | 1088 | 171 | 1088 | 305 |
| ENST00000518074 | SPIDR | chr8 | 48353104 | + | ENST00000342116 | FNTA | chr8 | 42938261 | + | 1944 | 1088 | 171 | 1088 | 305 |
| ENST00000541342 | SPIDR | chr8 | 48353104 | + | ENST00000302279 | FNTA | chr8 | 42938261 | + | 1897 | 1033 | 146 | 1033 | 295 |
| ENST00000541342 | SPIDR | chr8 | 48353104 | + | ENST00000342116 | FNTA | chr8 | 42938261 | + | 1889 | 1033 | 146 | 1033 | 295 |
| 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 |
| ENST00000297423 | ENST00000302279 | SPIDR | chr8 | 48353104 | + | FNTA | chr8 | 42938261 | + | 0.01164885 | 0.98835117 |
| ENST00000297423 | ENST00000342116 | SPIDR | chr8 | 48353104 | + | FNTA | chr8 | 42938261 | + | 0.012028459 | 0.9879716 |
| ENST00000518074 | ENST00000302279 | SPIDR | chr8 | 48353104 | + | FNTA | chr8 | 42938261 | + | 0.002603931 | 0.9973961 |
| ENST00000518074 | ENST00000342116 | SPIDR | chr8 | 48353104 | + | FNTA | chr8 | 42938261 | + | 0.002649107 | 0.99735093 |
| ENST00000541342 | ENST00000302279 | SPIDR | chr8 | 48353104 | + | FNTA | chr8 | 42938261 | + | 0.002602462 | 0.99739754 |
| ENST00000541342 | ENST00000342116 | SPIDR | chr8 | 48353104 | + | FNTA | chr8 | 42938261 | + | 0.002661106 | 0.99733883 |
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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 >85789_85789_1_SPIDR-FNTA_SPIDR_chr8_48353104_ENST00000297423_FNTA_chr8_42938261_ENST00000302279_length(amino acids)=476AA_BP= MEAAPAPGTSPAAPPNSPGARGRATPQPRASSAEPPAPGKEARLSAGHSFRAPGPTRPSGRPWSAGAGEALPPAEAPPCARAPANGRARC GAPRWDGGALRRRCAQAALPEMPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPSLTAEE KTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDRAEASDCDEFEDDEGAVEISDCASCA SNQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTP ENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAG -------------------------------------------------------------- >85789_85789_2_SPIDR-FNTA_SPIDR_chr8_48353104_ENST00000297423_FNTA_chr8_42938261_ENST00000342116_length(amino acids)=476AA_BP= MEAAPAPGTSPAAPPNSPGARGRATPQPRASSAEPPAPGKEARLSAGHSFRAPGPTRPSGRPWSAGAGEALPPAEAPPCARAPANGRARC GAPRWDGGALRRRCAQAALPEMPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPSLTAEE KTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDRAEASDCDEFEDDEGAVEISDCASCA SNQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTP ENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAG -------------------------------------------------------------- >85789_85789_3_SPIDR-FNTA_SPIDR_chr8_48353104_ENST00000518074_FNTA_chr8_42938261_ENST00000302279_length(amino acids)=305AA_BP= MAQSLTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDRAEASDCDEFEDDEGAV EISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQK PTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQ -------------------------------------------------------------- >85789_85789_4_SPIDR-FNTA_SPIDR_chr8_48353104_ENST00000518074_FNTA_chr8_42938261_ENST00000342116_length(amino acids)=305AA_BP= MAQSLTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDRAEASDCDEFEDDEGAV EISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQK PTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQ -------------------------------------------------------------- >85789_85789_5_SPIDR-FNTA_SPIDR_chr8_48353104_ENST00000541342_FNTA_chr8_42938261_ENST00000302279_length(amino acids)=295AA_BP= MAQVWRRVSEHFWESETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDRAEASDCDEFEDDEGAVEISDCASCAS NQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPE NSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGL -------------------------------------------------------------- >85789_85789_6_SPIDR-FNTA_SPIDR_chr8_48353104_ENST00000541342_FNTA_chr8_42938261_ENST00000342116_length(amino acids)=295AA_BP= MAQVWRRVSEHFWESETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDRAEASDCDEFEDDEGAVEISDCASCAS NQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPE NSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGL -------------------------------------------------------------- |
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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/chr8:42932507/chr8:48192450) - 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 |
| SPIDR | FNTA |
| FUNCTION: Plays a role in DNA double-strand break (DBS) repair via homologous recombination (HR). Serves as a scaffolding protein that helps to promote the recruitment of DNA-processing enzymes like the helicase BLM and recombinase RAD51 to site of DNA damage, and hence contributes to maintain genomic integrity. {ECO:0000269|PubMed:23509288, ECO:0000269|PubMed:23754376}. | FUNCTION: Essential subunit of both the farnesyltransferase and the geranylgeranyltransferase complex. Contributes to the transfer of a farnesyl or geranylgeranyl moiety from farnesyl or geranylgeranyl diphosphate to a cysteine at the fourth position from the C-terminus of several proteins having the C-terminal sequence Cys-aliphatic-aliphatic-X. May positively regulate neuromuscular junction development downstream of MUSK via its function in RAC1 prenylation and activation. {ECO:0000269|PubMed:12036349, ECO:0000269|PubMed:12825937, ECO:0000269|PubMed:16893176, ECO:0000269|PubMed:19246009, ECO:0000269|PubMed:8419339, ECO:0000269|PubMed:8494894}. |
| 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 |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000342116 | 3 | 7 | 216_249 | 193.66666666666666 | 313.0 | Repeat | Note=PFTA 4 | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000342116 | 3 | 7 | 255_289 | 193.66666666666666 | 313.0 | Repeat | Note=PFTA 5 |
| - 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 |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000302279 | 5 | 9 | 22_31 | 260.6666666666667 | 380.0 | Compositional bias | Note=Pro-rich | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000342116 | 3 | 7 | 22_31 | 193.66666666666666 | 313.0 | Compositional bias | Note=Pro-rich | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000302279 | 5 | 9 | 112_146 | 260.6666666666667 | 380.0 | Repeat | Note=PFTA 1 | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000302279 | 5 | 9 | 147_180 | 260.6666666666667 | 380.0 | Repeat | Note=PFTA 2 | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000302279 | 5 | 9 | 181_215 | 260.6666666666667 | 380.0 | Repeat | Note=PFTA 3 | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000302279 | 5 | 9 | 216_249 | 260.6666666666667 | 380.0 | Repeat | Note=PFTA 4 | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000302279 | 5 | 9 | 255_289 | 260.6666666666667 | 380.0 | Repeat | Note=PFTA 5 | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000342116 | 3 | 7 | 112_146 | 193.66666666666666 | 313.0 | Repeat | Note=PFTA 1 | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000342116 | 3 | 7 | 147_180 | 193.66666666666666 | 313.0 | Repeat | Note=PFTA 2 | |
| Tgene | FNTA | chr8:48353104 | chr8:42938261 | ENST00000342116 | 3 | 7 | 181_215 | 193.66666666666666 | 313.0 | Repeat | Note=PFTA 3 |
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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 |
| SPIDR | |
| FNTA |
| - 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 |
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Related Drugs to SPIDR-FNTA |
| 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 SPIDR-FNTA |
| 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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