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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Cfp and X-linked properdin deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with CFP (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to X-linked properdin deficiency  (DOID:0111768)
  • 6 papers in RGD have been used to annotate Cfp
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:8530058 PMID:10909851


  • An association has been curated linking Cfp and X-linked properdin deficiency 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 CFP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked properdin deficiency  (DOID:0111768)
  • 6 papers in RGD have been used to annotate Cfp


  • An association has been curated linking Cfp and X-linked properdin deficiency 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 CFP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-linked properdin deficiency  (DOID:0111768)
  • 6 papers in RGD have been used to annotate Cfp
  • Curation Notes: ClinVar Annotator: match by term: CFP-related condition | ClinVar Annotator: match by term: Properdin deficiency, X-linked | ClinVar Annotator: match by term: Properdin deficiency, type II | ClinVar Annotator: match by term: Properdin deficiency, type III
  • Original References(s): PMID:10909851 PMID:25741868 PMID:28492532 PMID:3380115 PMID:7151327 PMID:8530058 PMID:8871668


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