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Fusion Protein:RQCD1-CYP27A1 |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: RQCD1-CYP27A1 | FusionPDB ID: 78254 | FusionGDB2.0 ID: 78254 | Hgene | Tgene | Gene symbol | RQCD1 | CYP27A1 | Gene ID | 9125 | 1593 |
| Gene name | CCR4-NOT transcription complex subunit 9 | cytochrome P450 family 27 subfamily A member 1 | |
| Synonyms | CAF40|CT129|RCD-1|RCD1|RQCD1 | CP27|CTX|CYP27 | |
| Cytomap | 2q35 | 2q35 | |
| Type of gene | protein-coding | protein-coding | |
| Description | CCR4-NOT transcription complex subunit 9RCD1 required for cell differentiation1 homologcancer/testis antigen 129cell differentiation protein RCD1 homologcell differentiation protein RQCD1 homologprotein involved in sexual development | sterol 26-hydroxylase, mitochondrial5-beta-cholestane-3-alpha, 7-alpha, 12-alpha-triol 26-hydroxylase5-beta-cholestane-3-alpha, 7-alpha, 12-alpha-triol 27-hydroxylasecholestanetriol 26-monooxygenasecytochrome P-450C27/25cytochrome P450 27cytochrome | |
| Modification date | 20200313 | 20200320 | |
| UniProtAcc | . | Q02318 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000489687, ENST00000273064, ENST00000295701, ENST00000509807, ENST00000542068, | ENST00000258415, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 4 X 3 X 5=60 | 6 X 7 X 4=168 |
| # samples | 6 | 7 | |
| ** MAII score | log2(6/60*10)=0 | log2(7/168*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: RQCD1 [Title/Abstract] AND CYP27A1 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | RQCD1(219433701)-CYP27A1(219674300), # samples:1 RQCD1(219433701)-CYP27A1(219676945), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | RQCD1-CYP27A1 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. RQCD1-CYP27A1 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. RQCD1-CYP27A1 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF. RQCD1-CYP27A1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. RQCD1-CYP27A1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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 | RQCD1 | GO:2000327 | positive regulation of nuclear receptor transcription coactivator activity | 18180299 |
| Tgene | CYP27A1 | GO:0006699 | bile acid biosynthetic process | 9660774|11412116 |
| Tgene | CYP27A1 | GO:0006707 | cholesterol catabolic process | 9660774 |
| Tgene | CYP27A1 | GO:0036378 | calcitriol biosynthetic process from calciol | 15465040 |
| Fusion gene breakpoints across RQCD1 (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 CYP27A1 (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 | KIRC | TCGA-BP-4354-01A | RQCD1 | chr2 | 219433701 | + | CYP27A1 | chr2 | 219674300 | + |
| ChimerDB4 | KIRC | TCGA-BP-4354-01A | RQCD1 | chr2 | 219433701 | + | CYP27A1 | chr2 | 219676945 | + |
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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) |
| ENST00000509807 | RQCD1 | chr2 | 219433701 | + | ENST00000258415 | CYP27A1 | chr2 | 219674300 | + | 2003 | 399 | 168 | 1739 | 523 |
| ENST00000273064 | RQCD1 | chr2 | 219433701 | + | ENST00000258415 | CYP27A1 | chr2 | 219674300 | + | 2003 | 399 | 168 | 1739 | 523 |
| ENST00000542068 | RQCD1 | chr2 | 219433701 | + | ENST00000258415 | CYP27A1 | chr2 | 219674300 | + | 1875 | 271 | 40 | 1611 | 523 |
| ENST00000295701 | RQCD1 | chr2 | 219433701 | + | ENST00000258415 | CYP27A1 | chr2 | 219674300 | + | 1708 | 104 | 50 | 1444 | 464 |
| 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 |
| ENST00000509807 | ENST00000258415 | RQCD1 | chr2 | 219433701 | + | CYP27A1 | chr2 | 219674300 | + | 0.007831016 | 0.99216896 |
| ENST00000273064 | ENST00000258415 | RQCD1 | chr2 | 219433701 | + | CYP27A1 | chr2 | 219674300 | + | 0.007831016 | 0.99216896 |
| ENST00000542068 | ENST00000258415 | RQCD1 | chr2 | 219433701 | + | CYP27A1 | chr2 | 219674300 | + | 0.00885094 | 0.99114907 |
| ENST00000295701 | ENST00000258415 | RQCD1 | chr2 | 219433701 | + | CYP27A1 | chr2 | 219674300 | + | 0.012106344 | 0.98789364 |
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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 >78254_78254_1_RQCD1-CYP27A1_RQCD1_chr2_219433701_ENST00000273064_CYP27A1_chr2_219674300_ENST00000258415_length(amino acids)=523AA_BP=1 MGLLTRPWRREEDVWVGSGVRGQRAAKWAERAGVGWRLRRLIVFRCRGAEGGTRVGRVRLWKRAAAAHNMHSLATAAVLYKAKYGPMWMS YLGPQMHVNLASAPLLEQVMRQEGKYPVRNDMELWKEHRDQHDLTYGPFTTEGHHWYQLRQALNQRLLKPAEAALYTDAFNEVIDDFMTR LDQLRAESASGNQVSDMAQLFYYFALEAICYILFEKRIGCLQRSIPEDTVTFVRSIGLMFQNSLYATFLPKWTRPVLPFWKRYLDGWNAI FSFGKKLIDEKLEDMEAQLQAAGPDGIQVSGYLHFLLASGQLSPREAMGSLPELLMAGVDTTSNTLTWALYHLSKDPEIQEALHEEVVGV VPAGQVPQHKDFAHMPLLKAVLKETLRLYPVVPTNSRIIEKEIEVDGFLFPKNTQFVFCHYVVSRDPTAFSEPESFQPHRWLRNSQPATP -------------------------------------------------------------- >78254_78254_2_RQCD1-CYP27A1_RQCD1_chr2_219433701_ENST00000295701_CYP27A1_chr2_219674300_ENST00000258415_length(amino acids)=464AA_BP=1 MWKRAAAAHNMHSLATAAVLYKAKYGPMWMSYLGPQMHVNLASAPLLEQVMRQEGKYPVRNDMELWKEHRDQHDLTYGPFTTEGHHWYQL RQALNQRLLKPAEAALYTDAFNEVIDDFMTRLDQLRAESASGNQVSDMAQLFYYFALEAICYILFEKRIGCLQRSIPEDTVTFVRSIGLM FQNSLYATFLPKWTRPVLPFWKRYLDGWNAIFSFGKKLIDEKLEDMEAQLQAAGPDGIQVSGYLHFLLASGQLSPREAMGSLPELLMAGV DTTSNTLTWALYHLSKDPEIQEALHEEVVGVVPAGQVPQHKDFAHMPLLKAVLKETLRLYPVVPTNSRIIEKEIEVDGFLFPKNTQFVFC HYVVSRDPTAFSEPESFQPHRWLRNSQPATPRIQHPFGSVPFGYGVRACLGRRIAELEMQLLLARLIQKYKVVLAPETGELKSVARIVLV -------------------------------------------------------------- >78254_78254_3_RQCD1-CYP27A1_RQCD1_chr2_219433701_ENST00000509807_CYP27A1_chr2_219674300_ENST00000258415_length(amino acids)=523AA_BP=1 MGLLTRPWRREEDVWVGSGVRGQRAAKWAERAGVGWRLRRLIVFRCRGAEGGTRVGRVRLWKRAAAAHNMHSLATAAVLYKAKYGPMWMS YLGPQMHVNLASAPLLEQVMRQEGKYPVRNDMELWKEHRDQHDLTYGPFTTEGHHWYQLRQALNQRLLKPAEAALYTDAFNEVIDDFMTR LDQLRAESASGNQVSDMAQLFYYFALEAICYILFEKRIGCLQRSIPEDTVTFVRSIGLMFQNSLYATFLPKWTRPVLPFWKRYLDGWNAI FSFGKKLIDEKLEDMEAQLQAAGPDGIQVSGYLHFLLASGQLSPREAMGSLPELLMAGVDTTSNTLTWALYHLSKDPEIQEALHEEVVGV VPAGQVPQHKDFAHMPLLKAVLKETLRLYPVVPTNSRIIEKEIEVDGFLFPKNTQFVFCHYVVSRDPTAFSEPESFQPHRWLRNSQPATP -------------------------------------------------------------- >78254_78254_4_RQCD1-CYP27A1_RQCD1_chr2_219433701_ENST00000542068_CYP27A1_chr2_219674300_ENST00000258415_length(amino acids)=523AA_BP=1 MGLLTRPWRREEDVWVGSGVRGQRAAKWAERAGVGWRLRRLIVFRCRGAEGGTRVGRVRLWKRAAAAHNMHSLATAAVLYKAKYGPMWMS YLGPQMHVNLASAPLLEQVMRQEGKYPVRNDMELWKEHRDQHDLTYGPFTTEGHHWYQLRQALNQRLLKPAEAALYTDAFNEVIDDFMTR LDQLRAESASGNQVSDMAQLFYYFALEAICYILFEKRIGCLQRSIPEDTVTFVRSIGLMFQNSLYATFLPKWTRPVLPFWKRYLDGWNAI FSFGKKLIDEKLEDMEAQLQAAGPDGIQVSGYLHFLLASGQLSPREAMGSLPELLMAGVDTTSNTLTWALYHLSKDPEIQEALHEEVVGV VPAGQVPQHKDFAHMPLLKAVLKETLRLYPVVPTNSRIIEKEIEVDGFLFPKNTQFVFCHYVVSRDPTAFSEPESFQPHRWLRNSQPATP -------------------------------------------------------------- |
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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/chr2:219433701/chr2:219674300) - 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 |
| . | CYP27A1 |
| 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: Cytochrome P450 monooxygenase that catalyzes regio- and stereospecific hydroxylation of cholesterol and its derivatives. Hydroxylates (with R stereochemistry) the terminal methyl group of cholesterol side-chain in a three step reaction to yield at first a C26 alcohol, then a C26 aldehyde and finally a C26 acid (PubMed:9660774, PubMed:12077124, PubMed:21411718, PubMed:28190002). Regulates cholesterol homeostasis by catalyzing the conversion of excess cholesterol to bile acids via both the 'neutral' (classic) and the 'acid' (alternative) pathways (PubMed:9660774, PubMed:1708392, PubMed:11412116, PubMed:2019602, PubMed:7915755, PubMed:9186905, PubMed:9790667). May also regulate cholesterol homeostasis via generation of active oxysterols, which act as ligands for NR1H2 and NR1H3 nuclear receptors, modulating the transcription of genes involved in lipid metabolism (PubMed:9660774, PubMed:12077124). Plays a role in cholestanol metabolism in the cerebellum. Similarly to cholesterol, hydroxylates cholestanol and may facilitate sterol diffusion through the blood-brain barrier to the systemic circulation for further degradation (PubMed:28190002). Also hydroxylates retinal 7-ketocholesterol, a noxious oxysterol with pro-inflammatory and pro-apoptotic effects, and may play a role in its elimination from the retinal pigment epithelium (PubMed:21411718). May play a redundant role in vitamin D biosynthesis. Catalyzes 25-hydroxylation of vitamin D3 that is required for its conversion to a functionally active form (PubMed:15465040). {ECO:0000269|PubMed:11412116, ECO:0000269|PubMed:12077124, ECO:0000269|PubMed:15465040, ECO:0000269|PubMed:1708392, ECO:0000269|PubMed:2019602, ECO:0000269|PubMed:21411718, ECO:0000269|PubMed:28190002, ECO:0000269|PubMed:7915755, ECO:0000269|PubMed:9186905, ECO:0000269|PubMed:9660774, ECO:0000269|PubMed:9790667}. |
| 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 | CYP27A1 | chr2:219433701 | chr2:219674300 | ENST00000258415 | 0 | 9 | 384_398 | 85.0 | 532.0 | Region | Sterol-binding |
| - 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 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 |
| RQCD1 | |
| CYP27A1 |
| - 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 RQCD1-CYP27A1 |
| 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 RQCD1-CYP27A1 |
| 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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