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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking ERLIN2 and hereditary spastic paraplegia 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 ERLIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 453 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 0 papers in RGD have been used to annotate ERLIN2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia | ClinVar Annotator: match by term: Pure or complex autosomal recessive spastic paraplegia
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532 PMID:28832565 PMID:29528531 PMID:32042907 PMID:32147972 PMID:33397523 PMID:33810837 PMID:34734492 PMID:38427163


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