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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking SPAST and hereditary spastic paraplegia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11661564 (Homo sapiens)
  • 14 RGD objects have been annotated to hereditary spastic paraplegia 10  (DOID:0110763)
  • 6 papers in RGD have been used to annotate SPAST
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia, autosomal dominant
  • Original References(s): PMID:26467025 PMID:28492532


    • An association has been curated linking SPAST and hereditary spastic paraplegia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11583904 (Homo sapiens)
  • 14 RGD objects have been annotated to hereditary spastic paraplegia 10  (DOID:0110763)
  • 6 papers in RGD have been used to annotate SPAST
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia, autosomal dominant
  • Original References(s): PMID:25741868


    • An association has been curated linking SPAST and hereditary spastic paraplegia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11592540|RGD:11593600|RGD:11651131|RGD:11653665|RGD:11656618|RGD:11659680|RGD:11660316|RGD:11661425 (Homo sapiens) & RGD:11592540|RGD:11593600|RGD:11651131|RGD:11653665|RGD:11656618|RGD:11659680|RGD:11660316|RGD:11661425 (Homo sapiens) & RGD:11592540|RGD:11593600|RGD:11651131|RGD:11653665|RGD:11656618|RGD:11659680|RGD:11660316|RGD:11661425 (Homo sapiens) & RGD:11592540|RGD:11593600|RGD:11651131|RGD:11653665|RGD:11656618|RGD:11659680|RGD:11660316|RGD:11661425 (Homo sapiens) & RGD:11592540|RGD:11593600|RGD:11651131|RGD:11653665|RGD:11656618|RGD:11659680|RGD:11660316|RGD:11661425 (Homo sapiens) & RGD:11592540|RGD:11593600|RGD:11651131|RGD:11653665|RGD:11656618|RGD:11659680|RGD:11660316|RGD:11661425 (Homo sapiens) & RGD:11592540|RGD:11593600|RGD:11651131|RGD:11653665|RGD:11656618|RGD:11659680|RGD:11660316|RGD:11661425 (Homo sapiens) & RGD:11592540|RGD:11593600|RGD:11651131|RGD:11653665|RGD:11656618|RGD:11659680|RGD:11660316|RGD:11661425 (Homo sapiens)
  • 14 RGD objects have been annotated to hereditary spastic paraplegia 10  (DOID:0110763)
  • 6 papers in RGD have been used to annotate SPAST
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia, autosomal dominant


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