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HBA2 hemoglobin subunit alpha 2

Gene ID: 3040, updated on 30-Oct-2024
Gene type: protein coding
Also known as: HBH; ECYT7; HBA-T2

Summary

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) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported. [provided by RefSeq, Jul 2008]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
alpha Thalassemia
MedGen: C0002312OMIM: 604131GeneReviews: Alpha-Thalassemia
See labs
Erythrocytosis, familial, 7
MedGen: C4693823OMIM: 617981GeneReviews: Not available
See labs
Genome-wide association study of hematological and biochemical traits in a Japanese population.
GeneReviews: Not available
Heinz body anemia
MedGen: C0700299OMIM: 140700GeneReviews: Not available
See labs
Hemoglobin H disease
MedGen: C3161174OMIM: 613978GeneReviews: Not available
See labs

Genomic context

Location:
16p13.3
Sequence:
Chromosome: 16; NC_000016.10 (172876..173710)
Total number of exons:
3

Links

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