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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Uchl1 and hereditary spastic paraplegia 79A 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 UCHL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 79A  (DOID:0070455)
  • 20 papers in RGD have been used to annotate Uchl1


    • An association has been curated linking Uchl1 and hereditary spastic paraplegia 79A 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 UCHL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 79A  (DOID:0070455)
  • 20 papers in RGD have been used to annotate Uchl1
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 79A, autosomal dominant, with ataxia
  • Original References(s): PMID:25741868 PMID:28492532 PMID:35986737 PMID:37650884


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