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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Oxr1 and cerebellar hyplasia/atrophy, epilepsy, and global developmental delay in Ictidomys tridecemlineatus.        

  • 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 OXR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to cerebellar hyplasia/atrophy, epilepsy, and global developmental delay  (DOID:0070339)
  • 0 papers in RGD have been used to annotate Oxr1


    • An association has been curated linking Oxr1 and cerebellar hyplasia/atrophy, epilepsy, and global developmental delay in Ictidomys tridecemlineatus.        

  • 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 OXR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to cerebellar hyplasia/atrophy, epilepsy, and global developmental delay  (DOID:0070339)
  • 0 papers in RGD have been used to annotate Oxr1
  • Curation Notes: ClinVar Annotator: match by term: OXR1-related condition
  • Original References(s): PMID:25741868


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