SLC22A10
Description
The SLC22A10 (solute carrier family 22 member 10) is a protein-coding gene located on chromosome 11.
SLC22A10, also known as OAT5, is a protein encoded by the SLC22A10 gene in humans. This gene is involved in the transport of organic anions across cell membranes.
SLC22A10 is also known as OAT5, hOAT5.
Associated Diseases
- glycoprotein storage disease
- neuronal ceroid lipofuscinosis 1
- hemoglobin H disease
- hemoglobin C-beta-thalassemia syndrome
- combined immunodeficiency due to OX40 deficiency
- familial isolated congenital asplenia
- dominant beta-thalassemia
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- hereditary neutrophilia
- hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
- erythroleukemia, familial, susceptibility to
- beta-thalassemia-X-linked thrombocytopenia syndrome
- hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
