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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking FGFR1 and Pfeiffer syndrome in Canis lupus familiaris.        

  • 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Pfeiffer syndrome  (DOID:14705)
  • 0 papers in RGD have been used to annotate FGFR1


    • An association has been curated linking FGFR1 and Pfeiffer syndrome 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Pfeiffer syndrome  (DOID:14705)
  • 0 papers in RGD have been used to annotate FGFR1
  • Curation Notes: ClinVar Annotator: match by term: Acrocephalosyndactyly, type 5 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar Annotator: match by term: Pfeiffer syndrome type 1
  • Original References(s): PMID:10861678 PMID:10942429 PMID:11173846 PMID:14513299 PMID:1456217 PMID:14564217 PMID:14613973 PMID:15605412 PMID:15793702 PMID:16757108 PMID:16764984 PMID:16957473 PMID:17154279 PMID:18034870 PMID:18160472 PMID:18985070 PMID:20536592 PMID:20696889 PMID:23329143 PMID:23643382 PMID:23657145 PMID:23812909 PMID:24031091 PMID:24127277 PMID:24497711 PMID:25064402 PMID:25251565 PMID:25383892 PMID:25425165 PMID:25741868 PMID:25759380 PMID:26467025 PMID:26931467 PMID:26942290 PMID:28492532 PMID:28754744 PMID:31748124 PMID:31837199 PMID:33983622 PMID:7795583 PMID:7874169


    • An association has been curated linking FGFR1 and Pfeiffer syndrome 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 FGFR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Pfeiffer syndrome  (DOID:14705)
  • 0 papers in RGD have been used to annotate FGFR1
  • Curation Notes: ClinVar Annotator: match by term: Acrocephalosyndactyly, type 5 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar Annotator: match by term: Pfeiffer syndrome type 1
  • Original References(s): PMID:10861678 PMID:10942429 PMID:1456217 PMID:14564217 PMID:14613973 PMID:15605412 PMID:16764984 PMID:16957473 PMID:18034870 PMID:23643382 PMID:23657145 PMID:23812909 PMID:24127277 PMID:24497711 PMID:25064402 PMID:25251565 PMID:25741868 PMID:26931467 PMID:26942290 PMID:28492532 PMID:28754744 PMID:31837199 PMID:7795583 PMID:7874169


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