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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Actg1 and autosomal dominant nonsyndromic deafness 20 in Mus musculus.        

  • 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 ACTG1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 20  (DOID:0110550)
  • 11 papers in RGD have been used to annotate Actg1


    • An association has been curated linking Actg1 and autosomal dominant nonsyndromic deafness 20 in Mus musculus.        

  • 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 ACTG1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 20  (DOID:0110550)
  • 11 papers in RGD have been used to annotate Actg1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 20
  • Original References(s): PMID:12519370 PMID:13680526 PMID:14684684 PMID:16773128 PMID:17576681 PMID:18414213 PMID:19419963 PMID:19477959 PMID:19548389 PMID:20301607 PMID:22366783 PMID:23506231 PMID:24033266 PMID:25052316 PMID:25741868 PMID:25741909 PMID:25792668 PMID:26188271 PMID:26467025 PMID:27240540 PMID:28000701 PMID:28492532 PMID:29196752 PMID:29357087 PMID:29620237 PMID:29671837 PMID:29907799 PMID:29986705 PMID:30008475 PMID:30311386 PMID:30622556 PMID:31231230 PMID:32028042 PMID:32341388 PMID:33584783 PMID:33604570 PMID:35802133 PMID:36633841 PMID:5654493 PMID:9536098


    • An association has been curated linking Actg1 and autosomal dominant nonsyndromic deafness 20 in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with ACTG1 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 20  (DOID:0110550)
  • 11 papers in RGD have been used to annotate Actg1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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