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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Cwf19l1 and autosomal recessive spinocerebellar ataxia 17 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 CWF19L1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive spinocerebellar ataxia 17  (DOID:0080064)
  • 5 papers in RGD have been used to annotate Cwf19l1


    • An association has been curated linking Cwf19l1 and autosomal recessive spinocerebellar ataxia 17 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 CWF19L1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive spinocerebellar ataxia 17  (DOID:0080064)
  • 5 papers in RGD have been used to annotate Cwf19l1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive spinocerebellar ataxia 17 | ClinVar Annotator: match by term: CWF19L1-related condition
  • Original References(s): PMID:15981765 PMID:16199547 PMID:18414213 PMID:25361784 PMID:25741868 PMID:26197978 PMID:27016154 PMID:28492532


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