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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking MIR211 and congenital stationary night blindness 1C in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:21404361 (Homo sapiens)
  • 3 RGD objects have been annotated to congenital stationary night blindness 1C  (DOID:0110867)
  • 2 papers in RGD have been used to annotate MIR211
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness 1C
  • Original References(s): PMID:25741868


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