Basic Information
Regular Relationship :
Phenotype/DiseaseSpecieCerebellar Degeneration
CeRNA1CDR1-NAT[Circular RNA]
miRNAmiR-671[miRNA]
CeRNA2CDR1[mRNA]
Tissue/Cell lineHek293T
SpecieHomo sapiens (human)
CitationEmbo j 2011 Sep 30 30, 4414-22 doi:10.1038/emboj.2011.359 PMID:21964070
Reference title
miRNA-dependent gene silencing involving Ago2-mediated cleavage of a circular antisense RNA
Experimental verification
qRT-PCR;luciferase reporter assays
Functional description
Specifically, we show that miR-671 directs cleavage of a circular antisense transcript of the Cerebellar Degeneration-Related protein 1 (CDR1) locus in an Ago2-slicer-dependent manner. The resulting downregulation of circular antisense has a concomitant decrease in CDR1 mRNA levels, independently of heterochromatin formation.
Annotations
External Annotation for CDR1-NAT |
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LncRNA-associated competing triplets and functions. |
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Comprehensive experimentally supported associations between lncRNA and human cancer. |
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Infer genomic variations that disturb lncRNA-associated ceRNA regulation.. |
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Provide and annotate disease or phenotype-associated variants in human long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs) or their regulatory elements. |
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Providing cellular-specific lncRNA-associated ceRNA networks predicted via high-throughput analysis of single-cell genomic data. |
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Information on all annotated and predicted human genes. |
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Gene nomenclature, gene families and associated resources (genomic, proteomic, phenotypic information). |
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Genome browser for vertebrate genomes. |
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An annotated collection of all publicly available DNA sequences. |
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A wiki-based platform for community curation of human long non-coding RNAs. |
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An integrated knowledge database dedicated to non-coding RNAs. |
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An integrated database of human annotated lncRNA transcripts. |
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Comprehensive annotations of eukaryotic long non-coding RNAs. |
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Comprehensive experimentally supported associations between lncRNA and human cancer. |
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A comprehensive, authoritative compendium of human genes and genetic phenotypes. |
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The catalogue of somatic mutations in cancer. |
