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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:11026454


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: PCWH Syndrome
  • Original References(s): PMID:24033266, PMID:25741868


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:10762540


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:10482261, PMID:17855451


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease
  • Original References(s): PMID:25991456


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:12447940


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:15004559, PMID:19764030


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:10762540, PMID:15004559, PMID:1636383


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: PCWH Syndrome


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: PCWH Syndrome
  • Original References(s): PMID:24033266, PMID:25741868, PMID:9462749


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease
  • Original References(s): PMID:28492532


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease
  • Original References(s): PMID:22008330, PMID:24033266, PMID:28492532


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease
  • Original References(s): PMID:24033266, PMID:28492532


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease
  • Original References(s): PMID:25741868


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease
  • Original References(s): PMID:24033266, PMID:25741868, PMID:26467025


  • An association has been curated linking Polr2f and PCWH 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 POLR2F (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 CRRD objects have been annotated to PCWH syndrome  (DOID:0090111)
  • 14 papers in CRRD have been used to annotate Polr2f
  • Curation Notes: ClinVar Annotator: match by term: Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease
  • Original References(s): PMID:17999358, PMID:20127975, PMID:26467025, PMID:27240497, PMID:28492532


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