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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 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:12906096 (Homo sapiens)
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia-syndactyly syndrome 1
  • Original References(s): PMID:25529316


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 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:8602326 (Homo sapiens)
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia-syndactyly syndrome 1
  • Original References(s): PMID:21346770


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 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:8595424 (Homo sapiens)
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia-syndactyly syndrome 1
  • Original References(s): PMID:20691405 PMID:24577405


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 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:12905096 (Homo sapiens)
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia-syndactyly syndrome 1
  • Original References(s): PMID:24577405


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 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:21075030 (Homo sapiens)
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia-syndactyly syndrome 1


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 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:126733350|RGD:12899914 (Homo sapiens) & RGD:126733350|RGD:12899914 (Homo sapiens)
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia-syndactyly syndrome 1
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 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:126725480|RGD:243057393|RGD:42723648 (Homo sapiens) & RGD:126725480|RGD:243057393|RGD:42723648 (Homo sapiens) & RGD:126725480|RGD:243057393|RGD:42723648 (Homo sapiens)
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia-syndactyly syndrome 1
  • Original References(s): PMID:25741868


    • An association has been curated linking NECTIN4 and Ectodermal Dysplasia-Syndactyly Syndrome 1 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:8556343|RGD:8595423 (Homo sapiens) & RGD:8556343|RGD:8595423 (Homo sapiens)
  • 1 RGD objects have been annotated to Ectodermal Dysplasia-Syndactyly Syndrome 1  (DOID:9002370)
  • 6 papers in RGD have been used to annotate NECTIN4
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia-syndactyly syndrome 1
  • Original References(s): PMID:20691405


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