OSCP1
Description
The OSCP1 (organic solute carrier partner 1) is a protein-coding gene located on chromosome 1.
OSCP1 may play a role in eliminating drugs from the placenta.
OSCP1 is also known as C1orf102, NOR1.
Associated Diseases
- primary familial polycythemia due to EPO receptor mutation
- bipolar disorder
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- erythrocytosis, familial, 3
- erythrocytosis, familial, 6
- X-linked sideroblastic anemia 1
- cancer
- delta-beta-thalassemia
- anorexia nervosa
- schizophrenia
