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Hemoglobin Setif

Asp replaced by tyr position 94 on alpha chain

Also Known As:

Hb Setif

Networked: 4 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Blood Proteins: 12459
    - Hemoglobins: 37188
      - Abnormal Hemoglobins: 120
        Hemoglobin Setif: 4
  - Hemeproteins: 194
    - Globins: 2716
      - Hemoglobins: 37188
        Abnormal Hemoglobins: 120
        Hemoglobin Setif: 4

Experts

1.	Karimi, Mehran: 1 article (01/2011)
2.	Kosaryan, Mehrnoush: 1 article (01/2011)
3.	Mahdavi, Mohammad Reza: 1 article (01/2011)
4.	Roshan, Payam: 1 article (01/2011)
5.	Siami, Rita: 1 article (01/2011)
6.	Yavarian, Majid: 1 article (01/2011)
7.	Mozafari, Hadi: 1 article (01/2010)
8.	Muniz, Adriana: 1 article (01/2010)
9.	Rahimi, Zohreh: 1 article (01/2010)

Related Diseases

1.	beta-Thalassemia (Cooley's Anemia) 10/01/1983 - "Hemoglobin Setif and in vitro pseudosickling noted in a family with co-existent alpha and beta thalassemia." 05/01/1999 - "Quantification of Hb St. Luke's (11.1+/-1.12%) and Hb Setif (14.7+/-2.22%) in peripheral blood hemolysates indicated that, in the absence of either an alpha- or a beta-thalassemia allele, the protein products of the alpha1- and alpha2-globin genes were nearly equal in quantity."
2.	Hemoglobinopathies 01/01/2011 - "Hb Setif is a rare type of hemoglobinopathy resulting from an aspartic acid to tyrosine substitution at codon 94 (GAC>TAC) of the α2-globin gene. "
3.	Sickle Cell Anemia (Hemoglobin S Disease) 01/01/2010 - "We detected 28 subjects carrier for Hb D-Punjab (42.4%), 21 individuals carrier of Hb Q-Iran (31.8%), 12 subjects heterozygous for Hb Setif (18.2%), four cases with sickle cell disease (6.1%), and one case with Hb C (1.5%). "

Related Drugs and Biologics

1.	Tyrosine (L-Tyrosine)
2.	Proteins (Proteins, Gene)
3.	Codon (Codons)
4.	Aspartic Acid (Aspartate)
5.	hemoglobin Q Iran
6.	hemoglobin St. Luke's
7.	hemoglobin D Punjab