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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Hba-a1 and alpha thalassemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Liebhaber SA, etal., J Clin Invest. 1985 Sep;76(3):1057-64.
  • The annotation has been inferred from sequence orthology with HBA2 (Homo sapiens) [(IEP) inferred from expression pattern]
  • 5 additional annotations were made from Liebhaber SA, etal., J Clin Invest. 1985 Sep;76(3):1057-64.
  • 74 RGD objects have been annotated to alpha thalassemia  (DOID:1099)
  • 34 papers in RGD have been used to annotate Hba-a1


    • An association has been curated linking Hba-a1 and alpha thalassemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Morle F, etal., EMBO J. 1985 May;4(5):1245-50.
  • The annotation has been inferred from sequence orthology with HBA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Morle F, etal., EMBO J. 1985 May;4(5):1245-50.
  • 74 RGD objects have been annotated to alpha thalassemia  (DOID:1099)
  • 34 papers in RGD have been used to annotate Hba-a1
  • Curation Notes: DNA:deletion:cds:c.del-2_-3del(human)


    • An association has been curated linking Hba-a1 and alpha thalassemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Alauddin H, etal., Hemoglobin. 2014;38(4):277-81. doi: 10.3109/03630269.2014.916720. Epub 2014 May 14.
  • The annotation has been inferred from sequence orthology with HBA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Alauddin H, etal., Hemoglobin. 2014;38(4):277-81. doi: 10.3109/03630269.2014.916720. Epub 2014 May 14.
  • 74 RGD objects have been annotated to alpha thalassemia  (DOID:1099)
  • 34 papers in RGD have been used to annotate Hba-a1
  • Curation Notes: DNA:mutations:cds:c.179G>A (p.G60D);c.427¿¿¿T>C(human)


    • An association has been curated linking Hba-a1 and alpha thalassemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Mukherjee MB, etal., Indian J Med Res. 1998 Apr;107:178-81.
  • The annotation has been inferred from sequence orthology with HBA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Mukherjee MB, etal., Indian J Med Res. 1998 Apr;107:178-81.
  • 74 RGD objects have been annotated to alpha thalassemia  (DOID:1099)
  • 34 papers in RGD have been used to annotate Hba-a1
  • Qualifier: severity
  • Curation Notes: associated with Anemia, Sickle Cell;


    • An association has been curated linking Hba-a1 and alpha thalassemia in Rattus norvegicus.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Fucharoen S, etal., Haematologica. 2003 Oct;88(10):1092-8.
  • 5 additional annotations were made from Fucharoen S, etal., Haematologica. 2003 Oct;88(10):1092-8.
  • 74 RGD objects have been annotated to alpha thalassemia  (DOID:1099)
  • 34 papers in RGD have been used to annotate Hba-a1


    • An association has been curated linking Hba-a1 and alpha thalassemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Moi P, etal., J Clin Invest. 1987 Nov;80(5):1416-21.
  • The annotation has been inferred from sequence orthology with HBA2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Moi P, etal., J Clin Invest. 1987 Nov;80(5):1416-21.
  • 74 RGD objects have been annotated to alpha thalassemia  (DOID:1099)
  • 34 papers in RGD have been used to annotate Hba-a1
  • Curation Notes: DNA:missense mutation:cds: c.2T>C(human)


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