MOSPD1
Description
The MOSPD1 (motile sperm domain containing 1) is a protein-coding gene located on chromosome X.
MOSPD1 is also known as DJ473B4.
Associated Diseases
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- alpha thalassemia-intellectual disability syndrome type 1
- delta-beta-thalassemia
- hemoglobin D disease
- hemoglobin E-beta-thalassemia syndrome
- hemolytic anemia due to adenylate kinase deficiency
- hemoglobin C-beta-thalassemia syndrome
- alpha-thalassemia-myelodysplastic syndrome
- Heinz body anemia
- dominant beta-thalassemia
- hemoglobin H disease
- hemoglobin M disease
- hemoglobin E disease
- hereditary spherocytosis type 3
- pyropoikilocytosis, hereditary
