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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Slc17a8 and autosomal dominant nonsyndromic deafness 25 in Rattus norvegicus.        

  • 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 SLC17A8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 25  (DOID:0110555)
  • 26 papers in RGD have been used to annotate Slc17a8


  • An association has been curated linking Slc17a8 and autosomal dominant nonsyndromic deafness 25 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 SLC17A8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 25  (DOID:0110555)
  • 26 papers in RGD have been used to annotate Slc17a8
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 25
  • Original References(s): PMID:11115382 PMID:18674745 PMID:23967202 PMID:24033266 PMID:25741868 PMID:26467025 PMID:26797701 PMID:28492532 PMID:33229591


  • An association has been curated linking Slc17a8 and autosomal dominant nonsyndromic deafness 25 in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Slc17a8 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 25  (DOID:0110555)
  • 26 papers in RGD have been used to annotate Slc17a8
  • Curation Notes: OMIM:605583


  • An association has been curated linking Slc17a8 and autosomal dominant nonsyndromic deafness 25 in Rattus norvegicus.        

  • 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 SLC17A8 (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 25  (DOID:0110555)
  • 26 papers in RGD have been used to annotate Slc17a8
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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