ZNF729
Description
The ZNF729 (zinc finger protein 729) is a protein-coding gene located on chromosome 19.
Zinc finger protein 729 is a protein that in humans is encoded by the ZNF729 gene. It is a transcription factor that may play a role in the regulation of gene expression.
ZNF729 is also known as -.
Associated Diseases
- X-linked retinal dysplasia
- retinitis pigmentosa
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemoglobin D disease
- severe early-childhood-onset retinal dystrophy
- reticular dystrophy of the retinal pigment epithelium
- delta-beta-thalassemia
- dominant beta-thalassemia
- hemoglobin C-beta-thalassemia syndrome
- hemoglobin E-beta-thalassemia syndrome
- alpha-thalassemia-myelodysplastic syndrome
- X-linked retinoschisis
- retinitis pigmentosa and erythrocytic microcytosis
- hemoglobin E disease
