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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Pou4f3 and autosomal dominant nonsyndromic deafness 15 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with POU4F3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 15  (DOID:0110546)
  • 8 papers in RGD have been used to annotate Pou4f3


    • An association has been curated linking Pou4f3 and autosomal dominant nonsyndromic deafness 15 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 POU4F3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 15  (DOID:0110546)
  • 8 papers in RGD have been used to annotate Pou4f3
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 15
  • Original References(s): PMID:14585957 PMID:18228599 PMID:20434433 PMID:24033266 PMID:24260153 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29850532 PMID:30311386 PMID:32684921 PMID:32747562 PMID:9506947


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