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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking MYO6 and autosomal recessive nonsyndromic deafness 37 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 MYO6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 37  (DOID:0110495)
  • 0 papers in RGD have been used to annotate MYO6


    • An association has been curated linking MYO6 and autosomal recessive nonsyndromic deafness 37 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 MYO6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 37  (DOID:0110495)
  • 0 papers in RGD have been used to annotate MYO6
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 37 | ClinVar Annotator: match by term: MYO6-related condition
  • Original References(s): PMID:11167014 PMID:12687499 PMID:16199547 PMID:17576681 PMID:18212818 PMID:18348273 PMID:23767834 PMID:24033266 PMID:25080041 PMID:25741868 PMID:25741877 PMID:25999546 PMID:26445815 PMID:26467025 PMID:26944241 PMID:26969326 PMID:28492532 PMID:30311386 PMID:30582396 PMID:31589614 PMID:32143290 PMID:32747562 PMID:33279834 PMID:33724713 PMID:9536098


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