7qu4

Structural highlights

Disease

HBG2_HUMAN Hereditary persistence of fetal hemoglobin - beta-thalassemia;Hereditary persistence of fetal hemoglobin - sickle cell disease;Hemoglobinopathy Toms River. The disease is caused by mutations affecting the gene represented in this entry.

Function

HBG2_HUMAN Gamma chains make up the fetal hemoglobin F, in combination with alpha chains.