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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Slc11a2 and hypochromic anemia in Rattus norvegicus.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Fleming MD, etal., Proc Natl Acad Sci U S A 1998 Feb 3;95(3):1148-53.
  • 5 additional annotations were made from Fleming MD, etal., Proc Natl Acad Sci U S A 1998 Feb 3;95(3):1148-53.
  • 98 RGD objects have been annotated to hypochromic anemia  (DOID:11759)
  • 41 papers in RGD have been used to annotate Slc11a2
  • Curation Notes: DNA:missense mutation:cds:p.G185R (human)


    • An association has been curated linking Slc11a2 and hypochromic anemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Fleming MD, etal., Nat Genet. 1997 Aug;16(4):383-6.
  • The annotation has been inferred from sequence orthology with Slc11a2 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Fleming MD, etal., Nat Genet. 1997 Aug;16(4):383-6.
  • 98 RGD objects have been annotated to hypochromic anemia  (DOID:11759)
  • 41 papers in RGD have been used to annotate Slc11a2
  • Curation Notes: DNA:missense mutation:cds:p.G185R (human)


    • An association has been curated linking Slc11a2 and hypochromic anemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Beaumont C, etal., Blood. 2006 May 15;107(10):4168-70. Epub 2006 Jan 26.
  • The annotation has been inferred from sequence orthology with SLC11A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Beaumont C, etal., Blood. 2006 May 15;107(10):4168-70. Epub 2006 Jan 26.
  • 98 RGD objects have been annotated to hypochromic anemia  (DOID:11759)
  • 41 papers in RGD have been used to annotate Slc11a2
  • Curation Notes: DNA:deletion, missense mutation:cds:428_430delGTG, p.G212V (human)


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