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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking Cryl1 and autosomal dominant nonsyndromic deafness 3B 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 CRYL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 3B  (DOID:0110565)
  • 0 papers in RGD have been used to annotate Cryl1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 3b
  • Original References(s): PMID:27480936 PMID:28492532


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