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GENE - TERM ANNOTATION REPORT

40 Annotations Found.

An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by OMIM:615190
  • Original References(s): PMID:23453664


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by OMIM:615190
  • Original References(s): PMID:23329068


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by OMIM:615190
  • Original References(s): PMID:23591994


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:23453664, PMID:23959892, PMID:25607374, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:28492532, PMID:29344583


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532, PMID:29344583


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:27824607, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:25741868, PMID:28492532, PMID:29344583


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:23453664, PMID:26022962, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:27418648


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:28492532, PMID:30523160


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:23453664, PMID:25047097, PMID:25182133


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:25848748


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:28507545


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:26022962


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:28099038


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:25607374


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:27824607


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:25741868


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:26136524


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:23591994, PMID:28507545


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:25741868, PMID:27824607, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:27540018, PMID:28192371, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:23329068, PMID:25741868, PMID:27128385, PMID:28099038, PMID:28492532, PMID:28930861


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:25848748, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:23453664, PMID:24009516, PMID:24033266, PMID:25047097, PMID:25099625, PMID:25607374, PMID:25620558, PMID:26025130, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:23329068, PMID:23453664, PMID:23959892, PMID:24033266, PMID:25047097, PMID:25607374, PMID:28099038, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:23453664, PMID:23829372, PMID:24582487, PMID:27415407, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:26136524, PMID:28188499, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:28492532, PMID:29361909


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:25741868, PMID:27824607, PMID:28492532, PMID:29344583


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:28492532, PMID:28507545


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:24033266, PMID:25848748, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:24033266


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:24033266, PMID:28492532


  • An association has been curated linking Rtel1 and autosomal recessive dyskeratosis congenita 5 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 RTEL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to autosomal recessive dyskeratosis congenita 5  (DOID:0070022)
  • 5 papers in CRRD have been used to annotate Rtel1
  • Curation Notes: ClinVar Annotator: match by term: Dyskeratosis congenita, autosomal recessive, 5
  • Original References(s): PMID:19461895, PMID:23453664, PMID:23959892, PMID:26808564, PMID:27418648, PMID:28492532


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