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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Atrx and alpha-thalassemia myelodysplasia syndrome 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 ATRX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to alpha-thalassemia myelodysplasia syndrome  (DOID:0112125)
  • 32 papers in RGD have been used to annotate Atrx


  • An association has been curated linking Atrx and alpha-thalassemia myelodysplasia syndrome 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 ATRX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to alpha-thalassemia myelodysplasia syndrome  (DOID:0112125)
  • 32 papers in RGD have been used to annotate Atrx
  • Curation Notes: ClinVar Annotator: match by term: Acquired hemoglobin H disease | ClinVar Annotator: match by term: Alpha-thalassemia myelodysplasia syndrome
  • Original References(s): PMID:10995512 PMID:12858175 PMID:16955409 PMID:20500465 PMID:24327140 PMID:25590979 PMID:25741868 PMID:28492532 PMID:31130284 PMID:9326931


  • An association has been curated linking Atrx and alpha-thalassemia myelodysplasia syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with ATRX (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to alpha-thalassemia myelodysplasia syndrome  (DOID:0112125)
  • 32 papers in RGD have been used to annotate Atrx
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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