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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Myo6 and autosomal dominant nonsyndromic deafness 22 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 MYO6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 22  (DOID:0110552)
  • 22 papers in RGD have been used to annotate Myo6


    • An association has been curated linking Myo6 and autosomal dominant nonsyndromic deafness 22 in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Myo6 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 22  (DOID:0110552)
  • 22 papers in RGD have been used to annotate Myo6
  • Curation Notes: OMIM:606346


    • An association has been curated linking Myo6 and autosomal dominant nonsyndromic deafness 22 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 MYO6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 22  (DOID:0110552)
  • 22 papers in RGD have been used to annotate Myo6
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 22 | ClinVar Annotator: match by term: DFNA 22 | ClinVar Annotator: match by term: Deafness, autosomal dominant 22 | ClinVar Annotator: match by term: Deafness, autosomal dominant nonsyndromic sensorineural 22
  • Original References(s): PMID:11167014 PMID:11468689 PMID:12687499 PMID:15123708 PMID:16199547 PMID:17576681 PMID:18212818 PMID:18348273 PMID:21078986 PMID:23767834 PMID:24033266 PMID:24123366 PMID:25080041 PMID:25741868 PMID:25741877 PMID:25999546 PMID:26445815 PMID:26467025 PMID:26969326 PMID:26971995 PMID:28492532 PMID:28501645 PMID:29224747 PMID:30311386 PMID:30582396 PMID:31589614 PMID:32143290 PMID:32747562 PMID:33279834 PMID:33297549 PMID:33724713 PMID:35802133 PMID:35982127 PMID:36633841 PMID:36788145 PMID:9536098


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