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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Rint1 and Hereditary Neoplastic Syndromes 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 RINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1350 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 3 papers in RGD have been used to annotate Rint1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome
  • Original References(s): PMID:25050558 PMID:25741868 PMID:28492532 PMID:32566746


    • An association has been curated linking Rint1 and Hereditary Neoplastic Syndromes 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 RINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1350 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 3 papers in RGD have been used to annotate Rint1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary
  • Original References(s): PMID:17576681 PMID:24033266 PMID:25050558 PMID:25741868 PMID:26787654 PMID:26928227 PMID:27544226 PMID:28166811 PMID:28492532 PMID:31173646 PMID:31204009 PMID:31567591 PMID:32566746 PMID:33471991 PMID:9536098


    • An association has been curated linking Rint1 and Hereditary Neoplastic Syndromes 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 RINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1350 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 3 papers in RGD have been used to annotate Rint1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Hereditary neoplastic syndrome | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary
  • Original References(s): PMID:17576681 PMID:24033266 PMID:25050558 PMID:25741868 PMID:26787654 PMID:26928227 PMID:27544226 PMID:28166811 PMID:28492532 PMID:31173646 PMID:31204009 PMID:31567591 PMID:32283892 PMID:32566746 PMID:33099839 PMID:33471991 PMID:9536098


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