SLC22A25
Description
The SLC22A25 (solute carrier family 22 member 25) is a protein-coding gene located on chromosome 11.
SLC22A25, also known as organic anion transporter UST6, is a protein that in humans is encoded by the SLC22A25 gene.
SLC22A25 is also known as HIMTP, UST6.
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
- cryohydrocytosis
- thrombocytopenia, anemia, and myelofibrosis
- congenital dyserythropoietic anemia type 2
