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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking PTPRQ and autosomal dominant nonsyndromic deafness 73 in Canis lupus familiaris.        

  • 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 PTPRQ (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 73  (DOID:0080269)
  • 0 papers in RGD have been used to annotate PTPRQ


    • An association has been curated linking PTPRQ and autosomal dominant nonsyndromic deafness 73 in Canis lupus familiaris.        

  • 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 PTPRQ (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 73  (DOID:0080269)
  • 0 papers in RGD have been used to annotate PTPRQ
  • Curation Notes: ClinVar Annotator: match by term: DEAFNESS, AUTOSOMAL DOMINANT 73 | ClinVar Annotator: match by term: Deafness, autosomal dominant 73
  • Original References(s): PMID:25741868 PMID:26467025 PMID:29309402


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