Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:28492532


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 6
  • Original References(s): PMID:25893599


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by OMIM:616353
  • Original References(s): PMID:26342108


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:25741868, PMID:28414520, PMID:28492532


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:28414520, PMID:28492532


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:25741868


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:28099038, PMID:28492532


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:25848748, PMID:26810774, PMID:28492532, PMID:9736620


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:25741868, PMID:28492532, PMID:31448843


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:25741868, PMID:31448843


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:25848748, PMID:28492532


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:26482878, PMID:28414520, PMID:28492532


  • An association has been curated linking Parn and autosomal recessive dyskeratosis congenita 6 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with PARN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 6  (DOID:0070024)
  • 6 papers in CRRD have been used to annotate Parn
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive 6
  • Original References(s): PMID:25741868, PMID:26810774, PMID:28099038, PMID:28492532


  • Go Back to source page   Continue to Ontology report



    NHLBI Logo

    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.