HBAP1

From WikiMD's medical 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

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

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

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

References


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