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1 Annotations Found.

An association has been curated linking Slc17a8 and autosomal recessive nonsyndromic deafness 9 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 SLC17A8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 19 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 9  (DOID:0110535)
  • 26 papers in RGD have been used to annotate Slc17a8
  • Curation Notes: ClinVar Annotator: match by term: Auditory neuropathy spectrum disorder
  • Original References(s): PMID:27068579 PMID:28492532

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