Automated description from the Alliance of Genome Resources (Release 9.0.0)
Is expressed in blood; central nervous system; liver; and retina. Human ortholog(s) of this gene implicated in several diseases, including acute chest syndrome; congenital hemolytic anemia (multiple); polycythemia (multiple); sickle cell disease (multiple); and thalassemia (multiple). Orthologous to several human genes including HBB (hemoglobin subunit beta).
This site uses cookies.
Some cookies are essential for site operations and others help us analyze use and utility of our web site.
Please refer to our
privacy policy
for more information.