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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Cdc14a and autosomal recessive nonsyndromic deafness 32 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 CDC14A (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 32  (DOID:0110491)
  • 8 papers in RGD have been used to annotate Cdc14a
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:27259055 PMID:29293958


    • An association has been curated linking Cdc14a and autosomal recessive nonsyndromic deafness 32 in Mus musculus.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 32  (DOID:0110491)
  • 8 papers in RGD have been used to annotate Cdc14a
  • Curation Notes: OMIM:608653


    • An association has been curated linking Cdc14a and autosomal recessive nonsyndromic deafness 32 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 CDC14A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 32  (DOID:0110491)
  • 8 papers in RGD have been used to annotate Cdc14a


    • An association has been curated linking Cdc14a and autosomal recessive nonsyndromic deafness 32 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 CDC14A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 32  (DOID:0110491)
  • 8 papers in RGD have been used to annotate Cdc14a
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 105 | ClinVar Annotator: match by term: Deafness, autosomal recessive 32
  • Original References(s): PMID:12634867 PMID:24033266 PMID:25741868 PMID:27259055 PMID:28492532 PMID:29293958 PMID:31850270 PMID:31906439 PMID:32747562 PMID:34426522


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