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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:11348474


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:9008238


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:11348474, PMID:3954955


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:11886499, PMID:9008238


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:11886499


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:9767294


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:11874497


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:10571744


  • An association has been curated linking Krt17 and Pachyonychia Congenita 2 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 KRT17 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Pachyonychia Congenita 2  (DOID:9004213)
  • 8 papers in RGD have been used to annotate Krt17
  • Curation Notes: ClinVar Annotator: match by term: Pachyonychia congenita type 2
  • Original References(s): PMID:2248894, PMID:25741868, PMID:7529318, PMID:9008238, PMID:9767294


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.