Host: Mouse Monoclonal
The HBG1 gene codes for a 147 amino acid long, 16 kDA hemoglobin subunit gamma-1 protein that is typically found in fetal liver, spleen, and bone marrow. In conjunction with HBG2, they constitute fetal hemoglobin (HbF), which is eventually replaced at birth. HBG1 has been researched regarding various diseases such as sickle cell anemia, diabetes mellitus, anemia, leukemia, hemolytic anemia, thalassemia, spherocytosis, and hemoglobinopathy. HBG1 participates in IL-4 pathway, p70S6K signaling, and homeostasis and interacts with genes AHSP, HBA1, HBA2, CYB5R2, and GABARAPL2.
|Product By Gene ID
- hemoglobin, gamma, regulator of
- hemoglobin subunit gamma-1
- Hemoglobin gamma-A chain
- gamma globin
- Hemoglobin gamma-1 chain
- gamma A hemoglobin
- Hb F Agamma
- A-gamma globin
- hemoglobin, gamma A
Bioinformatics Tool for Hemoglobin gamma A
Discover related pathways, diseases and genes to Hemoglobin gamma A. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.