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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Fgfr3 and Muenke syndrome 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 FGFR3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muenke syndrome  (DOID:0060703)
  • 43 papers in RGD have been used to annotate Fgfr3


  • An association has been curated linking Fgfr3 and Muenke 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 FGFR3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muenke syndrome  (DOID:0060703)
  • 43 papers in RGD have been used to annotate Fgfr3
  • Curation Notes: ClinVar Annotator: match by term: Muenke syndrome
  • Original References(s): PMID:10053006, PMID:10094188, PMID:10213050, PMID:10602123, PMID:10777366, PMID:10861678, PMID:11424131, PMID:11746040, PMID:12707965, PMID:14613973, PMID:15241680, PMID:15915095, PMID:16501574, PMID:17033969, PMID:17935505, PMID:17950653, PMID:18000976, PMID:18328977, PMID:18344207, PMID:19098178, PMID:19215249, PMID:19449410, PMID:1956068, PMID:22045636, PMID:22604720, PMID:23165795, PMID:23378035, PMID:23740942, PMID:24728327, PMID:24864036, PMID:25356217, PMID:25741868, PMID:25931420, PMID:26028288, PMID:26740388, PMID:28492532, PMID:32238909, PMID:4078868, PMID:7670477, PMID:7847369, PMID:8723106, PMID:8841188, PMID:8845844, PMID:9042914, PMID:9107244, PMID:9279753, PMID:9279764, PMID:9450868, PMID:9525367, PMID:9580776, PMID:9585583, PMID:9600744, PMID:9677066, PMID:9843059, PMID:9950359


  • An association has been curated linking Fgfr3 and Muenke 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 FGFR3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muenke syndrome  (DOID:0060703)
  • 43 papers in RGD have been used to annotate Fgfr3
  • Curation Notes: ClinVar Annotator: match by term: Syndrome of coronal craniosynostosis
  • Original References(s): PMID:11055896, PMID:17875876, PMID:18583390, PMID:25741868, PMID:25809207, PMID:26818779, PMID:28492532


  • An association has been curated linking Fgfr3 and Muenke 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 FGFR3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muenke syndrome  (DOID:0060703)
  • 43 papers in RGD have been used to annotate Fgfr3
  • Curation Notes: ClinVar Annotator: match by term: Syndrome of coronal craniosynostosis
  • Original References(s): PMID:10471491, PMID:11038465, PMID:11879084, PMID:15772091, PMID:17384684, PMID:19381019, PMID:19749790, PMID:25157968, PMID:25606676, PMID:25741868, PMID:26619011, PMID:28492532, PMID:30311386, PMID:8589699


  • An association has been curated linking Fgfr3 and Muenke 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 FGFR3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muenke syndrome  (DOID:0060703)
  • 43 papers in RGD have been used to annotate Fgfr3
  • Curation Notes: ClinVar Annotator: match by term: Syndrome of coronal craniosynostosis
  • Original References(s): PMID:10073901, PMID:10471491, PMID:10696568, PMID:11241532, PMID:11529856, PMID:12833394, PMID:15772091, PMID:16841094, PMID:18642369, PMID:1908846, PMID:25157968, PMID:25606676, PMID:25741868, PMID:26619011, PMID:28492532, PMID:30311386, PMID:7773297, PMID:8858131, PMID:9677066


  • An association has been curated linking Fgfr3 and Muenke 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 FGFR3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muenke syndrome  (DOID:0060703)
  • 43 papers in RGD have been used to annotate Fgfr3
  • Curation Notes: ClinVar Annotator: match by term: Muenke syndrome


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.