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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking SUFU and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SUFU (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1239 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SUFU
  • Curation Notes: ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary
  • Original References(s): PMID:12068298 PMID:17102621 PMID:17576681 PMID:21188540 PMID:22508808 PMID:23826113 PMID:24728327 PMID:25287320 PMID:25403219 PMID:25741868 PMID:26184317 PMID:26467025 PMID:26580448 PMID:27363716 PMID:27930734 PMID:28050010 PMID:28166811 PMID:28492532 PMID:28717660 PMID:28873162 PMID:28965847 PMID:29641532 PMID:29654263 PMID:29753700 PMID:30256826 PMID:9536098


  • An association has been curated linking SUFU and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SUFU (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1239 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SUFU
  • 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:12068298 PMID:17102621 PMID:17576681 PMID:19533801 PMID:19833601 PMID:21188540 PMID:22508808 PMID:22958902 PMID:23826113 PMID:24651015 PMID:24728327 PMID:25287320 PMID:25403219 PMID:25741868 PMID:26467025 PMID:26580448 PMID:26677030 PMID:27363716 PMID:27930734 PMID:28050010 PMID:28492532 PMID:28717660 PMID:28873162 PMID:28965847 PMID:29186568 PMID:29641532 PMID:29654263 PMID:29753700 PMID:30256826 PMID:32295625 PMID:33024317 PMID:34056767 PMID:34589056 PMID:34675124 PMID:35768194 PMID:36825822 PMID:9536098


  • An association has been curated linking SUFU and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SUFU (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1239 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SUFU
  • 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
  • Original References(s): PMID:12068298 PMID:17102621 PMID:17576681 PMID:19533801 PMID:19833601 PMID:21188540 PMID:22508808 PMID:22958902 PMID:23826113 PMID:24651015 PMID:24728327 PMID:25287320 PMID:25403219 PMID:25741868 PMID:26467025 PMID:26580448 PMID:26677030 PMID:27363716 PMID:27793025 PMID:27930734 PMID:28050010 PMID:28492532 PMID:28717660 PMID:28873162 PMID:28965847 PMID:29186568 PMID:29641532 PMID:29654263 PMID:29753700 PMID:30256826 PMID:32295625 PMID:33024317 PMID:34056767 PMID:34589056 PMID:34675124 PMID:35768194 PMID:36825822 PMID:9536098


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