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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking ZNF469 and Brittle Cornea 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:11622165 (Homo sapiens)
  • 4 RGD objects have been annotated to Brittle Cornea Syndrome  (DOID:9005468)
  • 5 papers in RGD have been used to annotate ZNF469
  • Curation Notes: ClinVar Annotator: match by term: Brittle cornea syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28518168 PMID:29228253 PMID:32461654


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