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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking Greb1l and autosomal dominant nonsyndromic deafness 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 GREB1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 79 RGD objects have been annotated to autosomal dominant nonsyndromic deafness  (DOID:0050564)
  • 3 papers in RGD have been used to annotate Greb1l
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant non-syndromic sensorineural deafness type DFNA
  • Original References(s): PMID:25741868 PMID:32585897


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