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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Map2k2 and Noonan syndrome 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 MAP2K2 (Homo sapiens) [(EXP) inferred from experiment]
  • 54 RGD objects have been annotated to Noonan syndrome  (DOID:3490)
  • 29 papers in RGD have been used to annotate Map2k2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:17703371


    • An association has been curated linking Map2k2 and Noonan syndrome 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 MAP2K2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 54 RGD objects have been annotated to Noonan syndrome  (DOID:3490)
  • 29 papers in RGD have been used to annotate Map2k2
  • Curation Notes: ClinVar Annotator: match by term: Female pseudo-Turner syndrome | ClinVar Annotator: match by term: Noonan syndrome | ClinVar Annotator: match by term: Noonan's syndrome
  • Original References(s): PMID:17981815 PMID:18039235 PMID:18042262 PMID:18413255 PMID:18456719 PMID:19376813 PMID:22753777 PMID:23885229 PMID:24033266 PMID:25741868 PMID:25802880 PMID:28492532 PMID:29493581 PMID:29696744 PMID:30050098 PMID:30141192 PMID:30762279 PMID:33452774


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