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![]() | Fusion Gene Summary |
![]() | Fusion Gene ORF analysis |
![]() | Fusion Genomic Features |
![]() | Fusion Protein Features |
![]() | Fusion Gene Sequence |
![]() | Fusion Gene PPI analysis |
![]() | Related Drugs |
![]() | Related Diseases |
Fusion gene:CYC1-SLC52A2 (FusionGDB2 ID:HG1537TG79581) |
Fusion Gene Summary for CYC1-SLC52A2 |
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Fusion gene information | Fusion gene name: CYC1-SLC52A2 | Fusion gene ID: hg1537tg79581 | Hgene | Tgene | Gene symbol | CYC1 | SLC52A2 | Gene ID | 1537 | 79581 |
Gene name | cytochrome c1 | solute carrier family 52 member 2 | |
Synonyms | MC3DN6|UQCR4 | BVVLS2|D15Ertd747e|GPCR41|GPR172A|PAR1|RFT3|RFVT2|hRFT3 | |
Cytomap | ('CYC1')('SLC52A2') 8q24.3 | 8q24.3 | |
Type of gene | protein-coding | protein-coding | |
Description | cytochrome c1, heme protein, mitochondrialcomplex III subunit 4complex III subunit IVcytochrome b-c1 complex subunit 4cytochrome c-1ubiquinol-cytochrome-c reductase complex cytochrome c1 subunit | solute carrier family 52, riboflavin transporter, member 2G protein-coupled receptor 172APERV-A receptor 1porcine endogenous retrovirus A receptor 1putative G-protein coupled receptor GPCR41riboflavin transporter 3solute carrier family 52 (riboflavi | |
Modification date | 20200320 | 20200313 | |
UniProtAcc | P08574 | . | |
Ensembl transtripts involved in fusion gene | ENST00000318911, | ||
Fusion gene scores | * DoF score | 6 X 6 X 4=144 | 4 X 4 X 5=80 |
# samples | 6 | 5 | |
** MAII score | log2(6/144*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(5/80*10)=-0.678071905112638 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: CYC1 [Title/Abstract] AND SLC52A2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | CYC1(145151647)-SLC52A2(145582844), # samples:2 | ||
Anticipated loss of major functional domain due to fusion event. |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | SLC52A2 | GO:0032218 | riboflavin transport | 20463145|27702554 |
![]() * 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 | BLCA | TCGA-DK-A3IK-01A | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
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Fusion Gene ORF analysis for CYC1-SLC52A2 |
![]() * 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 |
5CDS-3UTR | ENST00000318911 | ENST00000526891 | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
5CDS-5UTR | ENST00000318911 | ENST00000329994 | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
5CDS-5UTR | ENST00000318911 | ENST00000402965 | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
5CDS-5UTR | ENST00000318911 | ENST00000526752 | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
5CDS-5UTR | ENST00000318911 | ENST00000527078 | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
5CDS-5UTR | ENST00000318911 | ENST00000530047 | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
5CDS-5UTR | ENST00000318911 | ENST00000532887 | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
5CDS-5UTR | ENST00000318911 | ENST00000540505 | CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582844 | + |
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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) |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for CYC1-SLC52A2 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582842 | + | 0.38842186 | 0.61157817 |
CYC1 | chr8 | 145151647 | + | SLC52A2 | chr8 | 145582842 | + | 0.38842186 | 0.61157817 |
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Fusion Protein Features for CYC1-SLC52A2 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:145151647/:145582844) - 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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Hgene | Tgene |
CYC1 | . |
FUNCTION: Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and the ATP synthase. The cytochrome b-c1 complex catalyzes electron transfer from ubiquinol to cytochrome c, linking this redox reaction to translocation of protons across the mitochondrial inner membrane, with protons being carried across the membrane as hydrogens on the quinol. In the process called Q cycle, 2 protons are consumed from the matrix, 4 protons are released into the intermembrane space and 2 electrons are passed to cytochrome c. Cytochrome c1 is a catalytic core subunit containing a c-type heme. It transfers electrons from the [2Fe-2S] iron-sulfur cluster of the Rieske protein to cytochrome c. {ECO:0000250|UniProtKB:P07143}. | FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. |
![]() * 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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Fusion Gene Sequence for CYC1-SLC52A2 |
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Fusion Gene PPI Analysis for CYC1-SLC52A2 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for CYC1-SLC52A2 |
![]() (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for CYC1-SLC52A2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | CYC1 | C3809553 | MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 | 1 | GENOMICS_ENGLAND;UNIPROT |
Tgene | C3553538 | BROWN-VIALETTO-VAN LAERE SYNDROME 2 | 9 | CLINGEN;GENOMICS_ENGLAND;UNIPROT | |
Tgene | C1849094 | SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3 | 1 | ORPHANET |