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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Atp13a2 and hereditary spastic paraplegia 78 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 ATP13A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 78  (DOID:0112348)
  • 9 papers in RGD have been used to annotate Atp13a2


    • An association has been curated linking Atp13a2 and hereditary spastic paraplegia 78 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 ATP13A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 78  (DOID:0112348)
  • 9 papers in RGD have been used to annotate Atp13a2
  • Curation Notes: ClinVar Annotator: match by term: ATP13A2-related condition | ClinVar Annotator: match by term: Autosomal recessive spastic paraplegia type 78
  • Original References(s): PMID:12169656 PMID:16964263 PMID:17576681 PMID:18075584 PMID:18075585 PMID:18414213 PMID:19085912 PMID:19458722 PMID:19705361 PMID:20683840 PMID:21060012 PMID:21665991 PMID:21696388 PMID:21724849 PMID:22296644 PMID:22442086 PMID:22768177 PMID:25466404 PMID:25741868 PMID:26467025 PMID:28137957 PMID:28492532 PMID:29966207 PMID:30833663 PMID:34382491 PMID:36703223 PMID:9536098


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