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1 Annotations Found.

An association has been curated linking Ppip5k1 and autosomal recessive nonsyndromic deafness 16 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 PPIP5K1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 16  (DOID:0110471)
  • 6 papers in RGD have been used to annotate Ppip5k1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 16
  • Original References(s): PMID:25741868

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