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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking LOC107126288 and Guttmacher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13831927|RGD:13832310|RGD:150446000|RGD:15108451|RGD:151809515|RGD:151823032|RGD:15192596 (Homo sapiens) & RGD:13831927|RGD:13832310|RGD:150446000|RGD:15108451|RGD:151809515|RGD:151823032|RGD:15192596 (Homo sapiens) & RGD:13831927|RGD:13832310|RGD:150446000|RGD:15108451|RGD:151809515|RGD:151823032|RGD:15192596 (Homo sapiens) & RGD:13831927|RGD:13832310|RGD:150446000|RGD:15108451|RGD:151809515|RGD:151823032|RGD:15192596 (Homo sapiens) & RGD:13831927|RGD:13832310|RGD:150446000|RGD:15108451|RGD:151809515|RGD:151823032|RGD:15192596 (Homo sapiens) & RGD:13831927|RGD:13832310|RGD:150446000|RGD:15108451|RGD:151809515|RGD:151823032|RGD:15192596 (Homo sapiens) & RGD:13831927|RGD:13832310|RGD:150446000|RGD:15108451|RGD:151809515|RGD:151823032|RGD:15192596 (Homo sapiens)
  • 2 RGD objects have been annotated to Guttmacher syndrome  (DOID:0111544)
  • 0 papers in RGD have been used to annotate LOC107126288
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias | ClinVar Annotator: match by term: Guttmacher syndrome
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LOC107126288 and Guttmacher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:150545807|RGD:150551516|RGD:150554229 (Homo sapiens) & RGD:150545807|RGD:150551516|RGD:150554229 (Homo sapiens) & RGD:150545807|RGD:150551516|RGD:150554229 (Homo sapiens)
  • 2 RGD objects have been annotated to Guttmacher syndrome  (DOID:0111544)
  • 0 papers in RGD have been used to annotate LOC107126288
  • Curation Notes: ClinVar Annotator: match by term: Guttmacher syndrome
  • Original References(s): PMID:25741868


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