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1 Annotations Found.

An association has been curated linking OPN1MW3 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:14351525 (Homo sapiens)
  • 2474 CRRD objects have been annotated to autistic disorder  (DOID:12849)
  • 1 papers in CRRD have been used to annotate OPN1MW3
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder of childhood onset
  • Original References(s): PMID:21681106, PMID:30208311

  • This annotation was curated on 2019-10-08 13:04:37.0 by CRRD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.