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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking C16orf92 and autistic disorder 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:14351735|RGD:14351741|RGD:14351747|RGD:14351752 (Homo sapiens) & RGD:14351735|RGD:14351741|RGD:14351747|RGD:14351752 (Homo sapiens) & RGD:14351735|RGD:14351741|RGD:14351747|RGD:14351752 (Homo sapiens) & RGD:14351735|RGD:14351741|RGD:14351747|RGD:14351752 (Homo sapiens)
  • 6366 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 2 papers in RGD have been used to annotate C16orf92
  • Curation Notes: ClinVar Annotator: match by term: Autism
  • Original References(s): PMID:21681106 PMID:30208311


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