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1 Annotations Found.

An association has been curated linking Myo15a and Deafness, with Smith-Magenis Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  • 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 from sequence orthology with MYO15A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Deafness, with Smith-Magenis Syndrome  (DOID:9007233)
  • 9 papers in RGD have been used to annotate Myo15a
  • Curation Notes: ClinVar Annotator: match by term: Deafness, with smith-magenis syndrome
  • Original References(s): PMID:11735029 PMID:17546645 PMID:19274735 PMID:24033266 PMID:28492532

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