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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Myh14 and autosomal dominant nonsyndromic deafness 4A 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 MYH14 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 4A  (DOID:0110573)
  • 9 papers in RGD have been used to annotate Myh14


    • An association has been curated linking Myh14 and autosomal dominant nonsyndromic deafness 4A 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 MYH14 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 4A  (DOID:0110573)
  • 9 papers in RGD have been used to annotate Myh14
  • Curation Notes: ClinVar Annotator: match by term: DEAFNESS, AUTOSOMAL DOMINANT 4A | ClinVar Annotator: match by term: Deafness, autosomal dominant 4A | ClinVar Annotator: match by term: MYH14-related condition
  • Original References(s): PMID:15015131 PMID:15845534 PMID:16222661 PMID:20533261 PMID:23967202 PMID:24033266 PMID:24082139 PMID:25741868 PMID:26284702 PMID:26346818 PMID:26467025 PMID:27393652 PMID:27610647 PMID:28166811 PMID:28221712 PMID:28492532 PMID:30311386 PMID:30828794 PMID:31231018 PMID:34681017


    • An association has been curated linking Myh14 and autosomal dominant nonsyndromic deafness 4A in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with MYH14 (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 4A  (DOID:0110573)
  • 9 papers in RGD have been used to annotate Myh14
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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