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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Aldh18a1 and hereditary spastic paraplegia 9B 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 ALDH18A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 9B  (DOID:0110825)
  • 15 papers in RGD have been used to annotate Aldh18a1


    • An association has been curated linking Aldh18a1 and hereditary spastic paraplegia 9B 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 ALDH18A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 9B  (DOID:0110825)
  • 15 papers in RGD have been used to annotate Aldh18a1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive complex spastic paraplegia type 9B | ClinVar Annotator: match by term: Spastic paraplegia 9b, autosomal recessive
  • Original References(s): PMID:17576681 PMID:25741868 PMID:26026163 PMID:26297558 PMID:26320891 PMID:28492532 PMID:29915212 PMID:32798076 PMID:36067040 PMID:37119015 PMID:37712079 PMID:9536098 PMID:9643297


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