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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking MIR6084 and Parkinson's disease 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11548616 (Homo sapiens)
  • 57 RGD objects have been annotated to Parkinson's disease 6  (DOID:0060369)
  • 0 papers in RGD have been used to annotate MIR6084
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking MIR6084 and Parkinson's disease 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156310415 (Homo sapiens)
  • 57 RGD objects have been annotated to Parkinson's disease 6  (DOID:0060369)
  • 0 papers in RGD have been used to annotate MIR6084
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6
  • Original References(s): PMID:28492532 PMID:30502028 PMID:32713623


    • An association has been curated linking MIR6084 and Parkinson's disease 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151812760 (Homo sapiens)
  • 57 RGD objects have been annotated to Parkinson's disease 6  (DOID:0060369)
  • 0 papers in RGD have been used to annotate MIR6084
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6
  • Original References(s): PMID:18330912 PMID:28492532


    • An association has been curated linking MIR6084 and Parkinson's disease 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12913711 (Homo sapiens)
  • 57 RGD objects have been annotated to Parkinson's disease 6  (DOID:0060369)
  • 0 papers in RGD have been used to annotate MIR6084
  • Curation Notes: ClinVar Annotator: match by term: PINK1-Related Parkinsonism
  • Original References(s): PMID:15349860 PMID:16009891 PMID:23063710 PMID:23303188 PMID:23459931 PMID:25741868 PMID:28492532 PMID:33845304


    • An association has been curated linking MIR6084 and Parkinson's disease 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15167991|RGD:152055389|RGD:152079207 (Homo sapiens) & RGD:15167991|RGD:152055389|RGD:152079207 (Homo sapiens) & RGD:15167991|RGD:152055389|RGD:152079207 (Homo sapiens)
  • 57 RGD objects have been annotated to Parkinson's disease 6  (DOID:0060369)
  • 0 papers in RGD have been used to annotate MIR6084
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking MIR6084 and Parkinson's disease 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11582284|RGD:151803472|RGD:156017931|RGD:156088796|RGD:156387591|RGD:28885713 (Homo sapiens) & RGD:11582284|RGD:151803472|RGD:156017931|RGD:156088796|RGD:156387591|RGD:28885713 (Homo sapiens) & RGD:11582284|RGD:151803472|RGD:156017931|RGD:156088796|RGD:156387591|RGD:28885713 (Homo sapiens) & RGD:11582284|RGD:151803472|RGD:156017931|RGD:156088796|RGD:156387591|RGD:28885713 (Homo sapiens) & RGD:11582284|RGD:151803472|RGD:156017931|RGD:156088796|RGD:156387591|RGD:28885713 (Homo sapiens) & RGD:11582284|RGD:151803472|RGD:156017931|RGD:156088796|RGD:156387591|RGD:28885713 (Homo sapiens)
  • 57 RGD objects have been annotated to Parkinson's disease 6  (DOID:0060369)
  • 0 papers in RGD have been used to annotate MIR6084
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6
  • Original References(s): PMID:28492532


    • An association has been curated linking MIR6084 and Parkinson's disease 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126728021|RGD:155697082 (Homo sapiens) & RGD:126728021|RGD:155697082 (Homo sapiens)
  • 57 RGD objects have been annotated to Parkinson's disease 6  (DOID:0060369)
  • 0 papers in RGD have been used to annotate MIR6084
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6
  • Original References(s): PMID:25741868


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