HBAP1

From WikiMD's Wellness Encyclopedia

HBAP1 is a gene that encodes a protein in humans. The protein is known as Hemoglobin Alpha Pseudogene 1 (HBAP1). This gene is located on chromosome 16 and is part of the hemoglobin gene family. Hemoglobin is a protein that carries oxygen in the red blood cells.

Function[edit | edit source]

The HBAP1 gene is a pseudogene of hemoglobin alpha. Pseudogenes are genes that have lost their protein-coding ability or are no longer expressed in the cell. The HBAP1 gene is believed to have no function due to its status as a pseudogene. However, some studies suggest that it may play a role in gene regulation and evolution.

Structure[edit | edit source]

The HBAP1 gene is located on the short (p) arm of chromosome 16 at position 13.3. The exact sequence of the HBAP1 gene is a subject of ongoing research, but it is known to be very similar to the hemoglobin alpha gene.

Clinical Significance[edit | edit source]

While the HBAP1 gene is generally considered to be non-functional, mutations in this gene have been associated with certain medical conditions. For example, a study found a correlation between mutations in the HBAP1 gene and the development of leukemia.

See Also[edit | edit source]

References[edit | edit source]


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