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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking PDZD7 and Usher Syndrome, Type 2B 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:8609070 (Homo sapiens)
  • 2 RGD objects have been annotated to Usher Syndrome, Type 2B  (DOID:9001128)
  • 6 papers in RGD have been used to annotate PDZD7
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PDZD7 and Usher Syndrome, Type 2B 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:14732739 (Homo sapiens)
  • 2 RGD objects have been annotated to Usher Syndrome, Type 2B  (DOID:9001128)
  • 6 papers in RGD have been used to annotate PDZD7
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2B
  • Original References(s): PMID:25741868


  • An association has been curated linking PDZD7 and Usher Syndrome, Type 2B 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:8606945 (Homo sapiens)
  • 2 RGD objects have been annotated to Usher Syndrome, Type 2B  (DOID:9001128)
  • 6 papers in RGD have been used to annotate PDZD7
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PDZD7 and Usher Syndrome, Type 2B 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:150455927 (Homo sapiens)
  • 2 RGD objects have been annotated to Usher Syndrome, Type 2B  (DOID:9001128)
  • 6 papers in RGD have been used to annotate PDZD7
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2B
  • Original References(s): PMID:25741868


  • An association has been curated linking PDZD7 and Usher Syndrome, Type 2B 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:8606950 (Homo sapiens)
  • 2 RGD objects have been annotated to Usher Syndrome, Type 2B  (DOID:9001128)
  • 6 papers in RGD have been used to annotate PDZD7
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PDZD7 and Usher Syndrome, Type 2B 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:11550193 (Homo sapiens)
  • 2 RGD objects have been annotated to Usher Syndrome, Type 2B  (DOID:9001128)
  • 6 papers in RGD have been used to annotate PDZD7
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PDZD7 and Usher Syndrome, Type 2B 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:8606942 (Homo sapiens)
  • 2 RGD objects have been annotated to Usher Syndrome, Type 2B  (DOID:9001128)
  • 6 papers in RGD have been used to annotate PDZD7
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2B
  • Original References(s): PMID:20440071 PMID:24033266 PMID:25741868 PMID:26849169 PMID:28492532


  • An association has been curated linking PDZD7 and Usher Syndrome, Type 2B 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:150543195 (Homo sapiens)
  • 2 RGD objects have been annotated to Usher Syndrome, Type 2B  (DOID:9001128)
  • 6 papers in RGD have been used to annotate PDZD7
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 2B
  • Original References(s): PMID:20440071 PMID:25741868 PMID:28492532 PMID:32050993


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