PRPF39
Description
The PRPF39 (pre-mRNA processing factor 39) is a protein-coding gene located on chromosome 14.
Plays a crucial role in the process of pre-mRNA splicing.
PRPF39 is also known as -.
Associated Diseases
- hemoglobin D disease
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemolytic anemia due to glutathione reductase deficiency
- dominant beta-thalassemia
- hemoglobin E-beta-thalassemia syndrome
- hemoglobin E disease
- delta-beta-thalassemia
- alpha-thalassemia-myelodysplastic syndrome
- hemoglobin C-beta-thalassemia syndrome
- primary familial polycythemia due to EPO receptor mutation
- hemoglobin H disease
- beta-thalassemia-X-linked thrombocytopenia syndrome
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- hemoglobin M disease
- monosomy 7 myelodysplasia and leukemia syndrome 1
