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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Ildr1 and autosomal recessive nonsyndromic deafness 42 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 ILDR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 42  (DOID:0110500)
  • 5 papers in RGD have been used to annotate Ildr1


    • An association has been curated linking Ildr1 and autosomal recessive nonsyndromic deafness 42 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 ILDR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 42  (DOID:0110500)
  • 5 papers in RGD have been used to annotate Ildr1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 42 | ClinVar Annotator: match by term: ILDR1-related condition
  • Original References(s): PMID:15641023 PMID:21255762 PMID:24033266 PMID:25668204 PMID:25741868 PMID:26226137 PMID:26467025 PMID:26969326 PMID:27610647 PMID:28492532 PMID:30303587 PMID:30311386 PMID:32747562


    • An association has been curated linking Ildr1 and autosomal recessive nonsyndromic deafness 42 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 Ildr1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 42  (DOID:0110500)
  • 5 papers in RGD have been used to annotate Ildr1
  • Curation Notes: OMIM:609646


    • An association has been curated linking Ildr1 and autosomal recessive nonsyndromic deafness 42 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 ILDR1 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 42  (DOID:0110500)
  • 5 papers in RGD have been used to annotate Ildr1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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