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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:C7orf73-PARK2 (FusionGDB2 ID:HG647087TG5071) |
Fusion Gene Summary for C7orf73-PARK2 |
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Fusion gene information | Fusion gene name: C7orf73-PARK2 | Fusion gene ID: hg647087tg5071 | Hgene | Tgene | Gene symbol | C7orf73 | PARK2 | Gene ID | 647087 | 5071 |
Gene name | short transmembrane mitochondrial protein 1 | parkin RBR E3 ubiquitin protein ligase | |
Synonyms | C7orf73|Mm47|PL-5283 | AR-JP|LPRS2|PARK2|PDJ | |
Cytomap | ('C7orf73')('PARK2') 7q33 | 6q26 | |
Type of gene | protein-coding | protein-coding | |
Description | short transmembrane mitochondrial protein 1uncharacterized protein C7orf73 | E3 ubiquitin-protein ligase parkinParkinson disease (autosomal recessive, juvenile) 2, parkinparkinson juvenile disease protein 2parkinson protein 2 E3 ubiquitin protein ligaseparkinson protein 2, E3 ubiquitin protein ligase (parkin) | |
Modification date | 20200313 | 20200329 | |
UniProtAcc | . | . | |
Ensembl transtripts involved in fusion gene | ENST00000422968, ENST00000507606, | ||
Fusion gene scores | * DoF score | 7 X 6 X 4=168 | 20 X 16 X 5=1600 |
# samples | 7 | 21 | |
** MAII score | log2(7/168*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(21/1600*10)=-2.9296106721086 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: C7orf73 [Title/Abstract] AND PARK2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | C7orf73(135359979)-PARK2(163132450), # samples:1 | ||
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 | PARK2 | GO:0000209 | protein polyubiquitination | 12150907|16227987|18541373|19880420 |
Tgene | PARK2 | GO:0000422 | autophagy of mitochondrion | 25621951 |
Tgene | PARK2 | GO:0001933 | negative regulation of protein phosphorylation | 17512523 |
Tgene | PARK2 | GO:0006511 | ubiquitin-dependent protein catabolic process | 12925569|17097639 |
Tgene | PARK2 | GO:0006513 | protein monoubiquitination | 20889974 |
Tgene | PARK2 | GO:0010506 | regulation of autophagy | 20889974 |
Tgene | PARK2 | GO:0010821 | regulation of mitochondrion organization | 21113145 |
Tgene | PARK2 | GO:0016567 | protein ubiquitination | 10973942|11439185|12628165|17314283 |
Tgene | PARK2 | GO:0031648 | protein destabilization | 19591802|29311685 |
Tgene | PARK2 | GO:0032232 | negative regulation of actin filament bundle assembly | 17512523 |
Tgene | PARK2 | GO:0033132 | negative regulation of glucokinase activity | 24187134 |
Tgene | PARK2 | GO:0043123 | positive regulation of I-kappaB kinase/NF-kappaB signaling | 17314283|19880420 |
Tgene | PARK2 | GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 11439185|21376232 |
Tgene | PARK2 | GO:0043388 | positive regulation of DNA binding | 17314283 |
Tgene | PARK2 | GO:0043524 | negative regulation of neuron apoptotic process | 12628165|22511790|23985028 |
Tgene | PARK2 | GO:0044828 | negative regulation by host of viral genome replication | 25244949 |
Tgene | PARK2 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 23453807 |
Tgene | PARK2 | GO:0046676 | negative regulation of insulin secretion | 24187134 |
Tgene | PARK2 | GO:0051865 | protein autoubiquitination | 12628165|15728840|16352719|17512523 |
Tgene | PARK2 | GO:0060548 | negative regulation of cell death | 15603737 |
Tgene | PARK2 | GO:0061734 | parkin-mediated stimulation of mitophagy in response to mitochondrial depolarization | 19029340 |
Tgene | PARK2 | GO:0070534 | protein K63-linked ubiquitination | 15728840|17314283|19880420|25621951 |
Tgene | PARK2 | GO:0070936 | protein K48-linked ubiquitination | 21376232|23858059 |
Tgene | PARK2 | GO:0070979 | protein K11-linked ubiquitination | 25621951 |
Tgene | PARK2 | GO:0085020 | protein K6-linked ubiquitination | 25621951 |
Tgene | PARK2 | GO:0090090 | negative regulation of canonical Wnt signaling pathway | 19591802 |
Tgene | PARK2 | GO:0090201 | negative regulation of release of cytochrome c from mitochondria | 19880420|23453807 |
Tgene | PARK2 | GO:0098779 | positive regulation of mitophagy in response to mitochondrial depolarization | 20457763 |
Tgene | PARK2 | GO:0099074 | mitochondrion to lysosome transport | 24446486 |
Tgene | PARK2 | GO:1900407 | regulation of cellular response to oxidative stress | 24446486 |
Tgene | PARK2 | GO:1902236 | negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway | 11439185|12150907|23453807 |
Tgene | PARK2 | GO:1903265 | positive regulation of tumor necrosis factor-mediated signaling pathway | 23453807 |
Tgene | PARK2 | GO:1903377 | negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway | 17314283 |
Tgene | PARK2 | GO:1903599 | positive regulation of autophagy of mitochondrion | 26310625 |
![]() * 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 |
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Fusion Gene ORF analysis for C7orf73-PARK2 |
![]() * 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 |
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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 C7orf73-PARK2 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
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Fusion Protein Features for C7orf73-PARK2 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:135359979/:163132450) - 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 |
. | . |
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}. | 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 C7orf73-PARK2 |
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Fusion Gene PPI Analysis for C7orf73-PARK2 |
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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 C7orf73-PARK2 |
![]() (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 C7orf73-PARK2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |