ZSWIM1
Description
The ZSWIM1 (zinc finger SWIM-type containing 1) is a protein-coding gene located on chromosome 20.
ZSWIM1 is also known as C20orf162.
Associated Diseases
- primary familial polycythemia due to EPO receptor mutation
- beta-thalassemia-X-linked thrombocytopenia syndrome
- neutrophil immunodeficiency syndrome
- alpha-thalassemia-myelodysplastic syndrome
- X-linked severe congenital neutropenia
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- neutropenia, severe congenital, 1, autosomal dominant
- hemoglobin D disease
- X-linked sideroblastic anemia 1
- gamma-glutamylcysteine synthetase deficiency
- dehydrated hereditary stomatocytosis
- alpha thalassemia-intellectual disability syndrome type 1
- pancytopenia-developmental delay syndrome
