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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking C8A and type I complement component 8 deficiency in Sus scrofa.        

  • 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 C8A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to type I complement component 8 deficiency  (DOID:0060301)
  • 0 papers in RGD have been used to annotate C8A


  • An association has been curated linking C8A and type I complement component 8 deficiency in Sus scrofa.        

  • 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 C8A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to type I complement component 8 deficiency  (DOID:0060301)
  • 0 papers in RGD have been used to annotate C8A
  • Curation Notes: ClinVar Annotator: match by term: COMPLEMENT COMPONENT 8, ALPHA SUBUNIT, A/B POLYMORPHISM | ClinVar Annotator: match by term: Type I complement component 8 deficiency
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:7649542 PMID:9759902


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