ZNF7
Description
The ZNF7 (zinc finger protein 7) is a protein-coding gene located on chromosome 8.
Zinc finger protein 7 is a protein encoded by the ZNF7 gene in humans. It has been shown to interact with the protein RPL7.
May be involved in regulating gene expression.
ZNF7 is also known as HF.16, KOX4, zf30.
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
