" /> HBA1 wt Allele - CISMeF





Preferred Label : HBA1 wt Allele;

NCIt synonyms : MGC126897; MGC126895; 3-Prime Alpha-Globin Gene; Alpha-1-Globin Gene; HBH; Hemoglobin Alpha 1 Globin Chain Gene; Alpha One Globin Gene; Hemoglobin Alpha-1 Chain Gene; Alpha-1 Globin Gene; HBA-T3; Hemoglobin-Alpha Locus 1 Gene; METHBA; Minor Alpha-Globin Locus; Hemoglobin, Alpha 1 Gene; Hemoglobin--Alpha Locus 1 Gene; Hemoglobin Subunit Alpha 1 wt Allele; 3' Alpha-Globin Gene; ECYT7;

NCIt definition : Human HBA1 wild-type allele is located in the vicinity of 16p13.3 and is approximately 1 kb in length. This allele, which encodes hemoglobin subunit alpha protein, plays a role in the regulation of vascular oxygen transport. Mutation or deletion of the gene is associated with alpha-thalassemia.;

NCIt note : The sequence of the coding region of the human HBA1 gene is identical to that of the human HBA2 gene. (Entrez Gene);

GenBank Accession Number : AF349571;

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12/05/2024


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