ARHGAP30
Description
The ARHGAP30 (Rho GTPase activating protein 30) is a protein-coding gene located on chromosome 1.
ARHGAP30 is also known as -.
Associated Diseases
- hemoglobin E-beta-thalassemia syndrome
- hemoglobin D disease
- beta-thalassemia-X-linked thrombocytopenia syndrome
- IRIDA syndrome
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- dominant beta-thalassemia
- Rh deficiency syndrome
- hemoglobin E disease
- hemoglobin C-beta-thalassemia syndrome
- delta-beta-thalassemia
- thrombocytopenia 2
- thrombocytopenia with congenital dyserythropoietic anemia
- alpha-thalassemia-myelodysplastic syndrome
