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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking SUV39H1 and X-linked severe congenital neutropenia 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:156441069 (Homo sapiens)
  • 94 RGD objects have been annotated to X-linked severe congenital neutropenia  (DOID:0112128)
  • 7 papers in RGD have been used to annotate SUV39H1
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe congenital neutropenia
  • Original References(s): PMID:28492532


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