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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Tecta and autosomal recessive nonsyndromic deafness 21 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 TECTA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 21  (DOID:0110479)
  • 9 papers in RGD have been used to annotate Tecta


  • An association has been curated linking Tecta and autosomal recessive nonsyndromic deafness 21 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 TECTA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 21  (DOID:0110479)
  • 9 papers in RGD have been used to annotate Tecta
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 21 | ClinVar Annotator: match by term: Deafness, neurosensory autosomal recessive 21 | ClinVar Annotator: match by term: TECTA-related condition
  • Original References(s): PMID:11087000 PMID:12746400 PMID:17431902 PMID:17576681 PMID:17661817 PMID:20947814 PMID:21520338 PMID:21917145 PMID:22718023 PMID:22980975 PMID:23967202 PMID:24033266 PMID:24130743 PMID:24586623 PMID:25262649 PMID:25741868 PMID:26467025 PMID:26969326 PMID:27068579 PMID:27627659 PMID:28000701 PMID:28492532 PMID:29196752 PMID:30303587 PMID:30311386 PMID:31163360 PMID:31554319 PMID:32747562 PMID:32853555 PMID:33111345 PMID:34008892 PMID:35802133 PMID:36633841 PMID:9536098 PMID:9949200


  • An association has been curated linking Tecta and autosomal recessive nonsyndromic deafness 21 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 TECTA (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 21  (DOID:0110479)
  • 9 papers in RGD have been used to annotate Tecta
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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