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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking LOC111982869 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:126909019 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 0 papers in RGD have been used to annotate LOC111982869
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868


  • An association has been curated linking LOC111982869 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:11604895 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 0 papers in RGD have been used to annotate LOC111982869
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking LOC111982869 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:11601276 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 0 papers in RGD have been used to annotate LOC111982869
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:28492532


  • An association has been curated linking LOC111982869 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8608905 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 0 papers in RGD have been used to annotate LOC111982869
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking LOC111982869 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:28905214 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 0 papers in RGD have been used to annotate LOC111982869
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:28492532


  • An association has been curated linking LOC111982869 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:151839546 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 0 papers in RGD have been used to annotate LOC111982869
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking LOC111982869 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:28905210 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 0 papers in RGD have been used to annotate LOC111982869
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:28492532


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