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  2. Hemoglobin subunit alpha - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_subunit_alpha

    The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 ( HBA2 ) and alpha-1 (HBA1; this gene) coding sequences are identical.

  3. Hemoglobin, alpha 2 - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin,_alpha_2

    The human alpha globin gene cluster is located on chromosome 16 and spans about 30 kb, including seven alpha like globin genes and pseudogenes: 5'- HBZ - HBZP1 - HBM - HBAP1 - HBA2 - HBA1 - HBQ1-3'. The HBA2 (α 2) and HBA1 (α 1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but ...

  4. Globin - Wikipedia

    en.wikipedia.org/wiki/Globin

    This 'globin fold' typically consists of eight alpha helices, although some proteins have additional helix extensions at their termini. [4] Since the globin fold contains only helices, it is classified as an all-alpha protein fold. The globin fold is found in its namesake globin families as well as in phycocyanins. The globin fold was thus the ...

  5. Hemoglobin A - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_A

    Globin synthesis takes place in the ribosomes which are located within the cytosol. Two globin chains that have heme groups combine to form hemoglobin. One of the chains is an alpha chain and the other is a non-alpha chain. Non-alpha chain nature in hemoglobin molecules varies due to different variables.

  6. Alpha-thalassemia - Wikipedia

    en.wikipedia.org/wiki/Alpha-thalassemia

    Alpha-thalassemia (α-thalassemia, α-thalassaemia) is a form of thalassemia involving the genes HBA1 [5] and HBA2. [6] Thalassemias are a group of inherited blood conditions which result in the impaired production of hemoglobin, the molecule that carries oxygen in the blood. [7]

  7. Hemoglobin - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin

    Alpha 1 and alpha 2 subunits are respectively coded by genes HBA1 and HBA2 close together on chromosome 16, while the beta subunit is coded by gene HBB on chromosome 11. The amino acid sequences of the globin subunits usually differ between species, with the difference growing with evolutionary distance.

  8. Hemoglobin variants - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_variants

    Hemoglobin variants occur when there are genetic changes in specific genes, or globins, that cause changes or alterations in the amino acid. They could affect the structure, behavior, the production rate, and/or the stability of that specific gene. Usually there are four genes that code for alpha globin and two genes that code for beta globin.

  9. Hemoglobin-G - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin-G

    Alpha Gene Arrangement Functioning α-genes Inheritance Hgb G, % Clinical Presentation uncomplicated G trait, no thalassemia: αG α/α α: 4: Mediterranean: 20-25: No defect alpha thal 2 with trans G trait: α -/αG – or – α/αG – 2: Mediterranean: 35-45: Microcytic alpha thal 2 trait, G trait: α3.7G/α α: 3: African American: 25-35 ...