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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Raf1 and Noonan syndrome 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 RAF1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Noonan syndrome 5  (DOID:0060583)
  • 45 papers in RGD have been used to annotate Raf1


  • An association has been curated linking Raf1 and Noonan syndrome 5 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with RAF1 (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to Noonan syndrome 5  (DOID:0060583)
  • 45 papers in RGD have been used to annotate Raf1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking Raf1 and Noonan syndrome 5 in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Raf1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Noonan syndrome 5  (DOID:0060583)
  • 45 papers in RGD have been used to annotate Raf1
  • Curation Notes: OMIM:611553


  • An association has been curated linking Raf1 and Noonan syndrome 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 RAF1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Noonan syndrome 5  (DOID:0060583)
  • 45 papers in RGD have been used to annotate Raf1
  • Curation Notes: ClinVar Annotator: match by term: Noonan syndrome 5
  • Original References(s): PMID:10064593 PMID:10497893 PMID:14701845 PMID:17576681 PMID:1760348 PMID:17603482 PMID:17603483 PMID:17603485 PMID:17603486 PMID:17603487 PMID:17603488 PMID:17603489 PMID:18241070 PMID:18505544 PMID:18553519 PMID:19568997 PMID:19723757 PMID:19933846 PMID:19953625 PMID:20052757 PMID:20301557 PMID:20679480 PMID:20683980 PMID:21339642 PMID:21440552 PMID:21784453 PMID:22389993 PMID:22465605 PMID:22558107 PMID:22781091 PMID:22821648 PMID:22824796 PMID:22826437 PMID:23312806 PMID:23321623 PMID:23737487 PMID:23877478 PMID:23885229 PMID:24033266 PMID:24775816 PMID:24777450 PMID:24803665 PMID:25706034 PMID:25741868 PMID:25862627 PMID:26266034 PMID:26467173 PMID:26580448 PMID:26619011 PMID:26659599 PMID:26918529 PMID:27631234 PMID:27753652 PMID:28492532 PMID:28777121 PMID:28973083 PMID:28991257 PMID:29084544 PMID:29232918 PMID:29271604 PMID:29493581 PMID:29522511 PMID:29907801 PMID:29948256 PMID:30055033 PMID:30105547 PMID:30138938 PMID:30384889 PMID:30417923 PMID:30732632 PMID:31324109 PMID:31395954 PMID:31560489 PMID:31589614 PMID:32269299 PMID:32410215 PMID:32506814 PMID:32573669 PMID:32668055 PMID:32981126 PMID:33240318 PMID:33318624 PMID:33673806 PMID:34006472 PMID:34136434 PMID:35050212 PMID:9536098


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