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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: KERATOSIS PALMOPLANTARIS WITH CYSTIC EYELIDS, HYPODONTIA, AND HYPOTRICHOSIS
  • Original References(s): PMID:28492532


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:25629078 PMID:25741868 PMID:28492532


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by OMIM:224750


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by OMIM:224750
  • Original References(s): PMID:21484994


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: KERATOSIS PALMOPLANTARIS WITH CYSTIC EYELIDS, HYPODONTIA, AND HYPOTRICHOSIS
  • Original References(s): PMID:17847007 PMID:20163410 PMID:22581971 PMID:23167694 PMID:25741868 PMID:28492532


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:22581971 PMID:23401279 PMID:24398796 PMID:28492532 PMID:30426266


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:23401279 PMID:24043634 PMID:24311251 PMID:24312213 PMID:25629078 PMID:25741868 PMID:28492532


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:24043634 PMID:24312213 PMID:25741868 PMID:28492532


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: KERATOSIS PALMOPLANTARIS WITH CYSTIC EYELIDS, HYPODONTIA, AND HYPOTRICHOSIS
  • Original References(s): PMID:24043634


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:17847007 PMID:19559398 PMID:21834823 PMID:22581971 PMID:23167694 PMID:23401279 PMID:24043634 PMID:24398796 PMID:24449199 PMID:24700731 PMID:24702986 PMID:24902757 PMID:25356970 PMID:25545742 PMID:25629078 PMID:25741868 PMID:28105635 PMID:28492532


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:25629078 PMID:28492532


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:20979233 PMID:28492532 PMID:28981473 PMID:30569517


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:22581971 PMID:23401279 PMID:28492532


  • An association has been curated linking Wnt10a and Schopf-Schulz-Passarge syndrome 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 WNT10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Schopf-Schulz-Passarge syndrome  (DOID:0111647)
  • 13 papers in RGD have been used to annotate Wnt10a
  • Curation Notes: ClinVar Annotator: match by term: Schopf-Schulz-Passarge syndrome
  • Original References(s): PMID:17847007 PMID:19559398 PMID:21484994 PMID:22581971 PMID:23401279 PMID:24033266 PMID:24449199 PMID:24700731 PMID:25629078 PMID:25741868 PMID:26964878 PMID:27881089 PMID:28166811 PMID:28492532 PMID:28813618 PMID:28976000 PMID:29364747 PMID:30426266 PMID:30974434


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