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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Col11a2 and autosomal dominant nonsyndromic deafness 13 in Ictidomys tridecemlineatus.        

  • 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 COL11A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 13  (DOID:0110545)
  • 0 papers in RGD have been used to annotate Col11a2


    • An association has been curated linking Col11a2 and autosomal dominant nonsyndromic deafness 13 in Ictidomys tridecemlineatus.        

  • 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 COL11A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 13  (DOID:0110545)
  • 0 papers in RGD have been used to annotate Col11a2
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 13
  • Original References(s): PMID:10581026 PMID:10677296 PMID:15372529 PMID:15558753 PMID:21204229 PMID:23967202 PMID:24033266 PMID:25633957 PMID:25741868 PMID:26969326 PMID:28492532 PMID:33105617 PMID:35802133 PMID:36633841


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