Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Rtn2 and hereditary spastic paraplegia 10 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 RTN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 RGD objects have been annotated to hereditary spastic paraplegia 10  (DOID:0110763)
  • 7 papers in RGD have been used to annotate Rtn2
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia, autosomal dominant


  • An association has been curated linking Rtn2 and hereditary spastic paraplegia 10 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 RTN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 RGD objects have been annotated to hereditary spastic paraplegia 10  (DOID:0110763)
  • 7 papers in RGD have been used to annotate Rtn2
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Rtn2 and hereditary spastic paraplegia 10 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 RTN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 RGD objects have been annotated to hereditary spastic paraplegia 10  (DOID:0110763)
  • 7 papers in RGD have been used to annotate Rtn2
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia, autosomal dominant
  • Original References(s): PMID:26467025 PMID:28492532


  • Go Back to source page   Continue to Ontology report