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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking GRHL3 and Van der Woude syndrome in Homo sapiens.        

  • 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 Grhl3 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 8 RGD objects have been annotated to Van der Woude syndrome  (DOID:0060239)
  • 4 papers in RGD have been used to annotate GRHL3
  • Curation Notes: OMIM:119300 | OMIM:606713


    • An association has been curated linking GRHL3 and Van der Woude 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:13517731 (Homo sapiens)
  • 8 RGD objects have been annotated to Van der Woude syndrome  (DOID:0060239)
  • 4 papers in RGD have been used to annotate GRHL3
  • Curation Notes: ClinVar Annotator: match by term: Van der Woude syndrome 1
  • Original References(s): PMID:25741868


    • An association has been curated linking GRHL3 and Van der Woude 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:401723989 (Homo sapiens)
  • 8 RGD objects have been annotated to Van der Woude syndrome  (DOID:0060239)
  • 4 papers in RGD have been used to annotate GRHL3
  • Curation Notes: ClinVar Annotator: match by term: Van der Woude syndrome
  • Original References(s): PMID:36901693


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