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GENE - TERM ANNOTATION REPORT

27 Annotations Found.

An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by OMIM:135290
  • Original References(s): PMID:10782927


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by OMIM:135290
  • Original References(s): PMID:10077730


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by OMIM:135290
  • Original References(s): PMID:8940264


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:12007223, PMID:12173026, PMID:1316610, PMID:15108286, PMID:16134147, PMID:17963004, PMID:18433509, PMID:20223039, PMID:20649969, PMID:20685668, PMID:20924072, PMID:21110124, PMID:24033266, PMID:24735542, PMID:25741868, PMID:26300997, PMID:26467025, PMID:28492532, PMID:9342373, PMID:9664575


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:25741868, PMID:25980754, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:15459959, PMID:17489848, PMID:19793053, PMID:20223039, PMID:20685668, PMID:22431159, PMID:23159591, PMID:24599579, PMID:25590978, PMID:25741868, PMID:28492532, PMID:8381580


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:10768871, PMID:12901799, PMID:1338764, PMID:20223039, PMID:20685668, PMID:20924072, PMID:25741868, PMID:28492532, PMID:8162022, PMID:8187091, PMID:9950360


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:25741868


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:25741868, PMID:26580448, PMID:26976419, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:10083733, PMID:10094547, PMID:10713886, PMID:11748858, PMID:11933206, PMID:12173026, PMID:1324223, PMID:15024739, PMID:15108288, PMID:15300853, PMID:15951963, PMID:16088911, PMID:16134147, PMID:16292097, PMID:16317745, PMID:17411426, PMID:17785554, PMID:18433509, PMID:19029688, PMID:19444466, PMID:1944466, PMID:19793053, PMID:20223039, PMID:20685668, PMID:20924072, PMID:23970361, PMID:24033266, PMID:25741868, PMID:26300997, PMID:26467025, PMID:26845104, PMID:28492532, PMID:8381579, PMID:8990002


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:12034871, PMID:16461775, PMID:18433509, PMID:20301519, PMID:24033266, PMID:25741868, PMID:25980754, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:24123366, PMID:25741868, PMID:25980754, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:17963004, PMID:20685668, PMID:25741868, PMID:28492532, PMID:8844222


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:18199528, PMID:21859464, PMID:21901162, PMID:24033266, PMID:25637381, PMID:25741868, PMID:25925381, PMID:26467025, PMID:26580448, PMID:26845104, PMID:27150160, PMID:28492532, PMID:29641532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:12357334, PMID:1324223, PMID:15108286, PMID:15951963, PMID:20223039, PMID:20685668, PMID:20924072, PMID:24033266, PMID:25741868, PMID:26613750, PMID:26845104, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:10094547, PMID:1316610, PMID:15024739, PMID:15857185, PMID:17411426, PMID:20223039, PMID:20685668, PMID:24033266, PMID:25525159, PMID:25741868, PMID:26138249, PMID:26681312, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:10083733, PMID:10470088, PMID:15108286, PMID:16088911, PMID:17411426, PMID:18433509, PMID:19029688, PMID:19531215, PMID:20223039, PMID:20685668, PMID:20924072, PMID:23159591, PMID:25741868, PMID:26446593, PMID:26467025, PMID:28492532, PMID:8187091


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:18433509, PMID:22703879, PMID:24033266, PMID:24728327, PMID:25741868, PMID:25801821, PMID:26467025, PMID:26580448, PMID:27600092, PMID:28492532, PMID:29915797, PMID:30374176, PMID:30613976


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:18199528, PMID:22703879, PMID:25741868, PMID:26320869, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:25741868, PMID:25992589, PMID:26493165, PMID:28492532


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:25186627, PMID:25741868, PMID:26467025, PMID:28135145, PMID:28492532, PMID:28608266


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:22703879, PMID:24448499, PMID:24573554, PMID:25186627, PMID:25741868, PMID:25980754, PMID:26467025, PMID:27600092, PMID:28135145, PMID:28492532, PMID:30374176, PMID:31428572


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:22703879, PMID:24728327, PMID:25203624, PMID:25479140, PMID:25741868, PMID:26467025, PMID:27153395, PMID:27878467, PMID:28492532, PMID:28873162, PMID:29684080, PMID:29945567


  • An association has been curated linking Apc and hereditary desmoid disease 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 APC (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to hereditary desmoid disease  (DOID:0111349)
  • 59 papers in CRRD have been used to annotate Apc
  • Curation Notes: ClinVar Annotator: match by term: Desmoid disease, hereditary
  • Original References(s): PMID:25186627, PMID:25741868, PMID:25980754, PMID:26467025, PMID:27978560, 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.